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CSQE Certified Software Quality Engineer Certification (CSQE)

The Certified Software Quality Engineer (CSQE) understands software quality development and implementation, software inspection, testing, and verification and validation; and implements software development and maintenance processes and methods.CSQEComputer Delivered – The CSQE examination is a one-part, 175-question, four-and-a-half-hour exam and is offered in English only. One hundred and sixty questions are scored and 15 are unscored.Paper and Pencil – The CSQEexamination is a one-part, 160-question, four-hour exam and is offered in English only.

Work experience must be in a full-time, paid role. Paid intern, co-op or any other course work cannot be applied toward the work experience requirement.

Candidates must have eight years of on-the-job experience in one or more of the areas of the Certified Software Quality Engineer Body of Knowledge.

A minimum of three years of this experience must be in a decision-making position. ("Decision-making" is defined as the authority to define, execute, or control projects/processes and to be responsible for the outcome. This may or may not include management or supervisory positions.)

For candidates who were certified by ASQ as a quality auditor, reliability engineer, supplier quality professional, quality engineer or quality manager, the experience used to qualify for certification in these fields applies to certification as a software quality engineer.

Here are the minimum expectations of a Certified Software Quality Engineer.
Must possess a fundamental understanding of quality philosophies, principles, methods, tools, standards, organizational and team dynamics, interpersonal relationships, professional ethics, and legal and regulatory requirements. Must evaluate the impact of software quality management principles on business objectives and demonstrate comprehensive knowledge of developing and implementing software quality programs, which include tracking, analyzing, reporting, problem resolution, process improvement, training, and supplier management. Must have a basic understanding of how and when to perform software audits including audit planning, approaches, types, analyses, reporting results and follow-up. Must understand systems architecture and be able to implement software development and maintenance processes, quantify the fundamental problems and risks associated with various software development methodologies, and assess, support, and implement process and technology changes.
Must be able to apply project management principles and techniques as they relate to software project planning, implementation and tracking. Must be able to evaluate and manage risk. Must select, define and apply product and process metrics and analytical techniques, and have an understanding of measurement theory and how to communicate results. Must have a thorough understanding of verification and validation processes, including early software defect detection and removal, inspection, and testing methods (e.g., types, levels, strategies, tools and documentation). Must be able to analyze test strategies, develop test plans and execution documents, and review customer deliverables. Must have a basic understanding of configuration management processes, including planning, configuration identification, configuration control, change management, status accounting, auditing and reporting. Must assess the effectiveness of product release and archival processes.

Certification from ASQ is considered a mark of quality excellence in many industries. It helps you advance your career, and boosts your organizations bottom line through your mastery of quality skills. Becoming certified as a Software Quality Engineer confirms your commitment to quality and the positive impact it will have on your organization. ExaminationEach certification candidate is required to pass an examination that consists of multiple-choice questions that measure comprehension of the body of knowledge.

I. General Knowledge (16 questions)A. Benefits of Software Quality Engineering Within the OrganizationDescribe the benefits that software quality engineering can have at the organizational level. (Understand)B. Ethical and Legal Compliance 1. ASQ code of ethics for professional conductDetermine appropriate behavior in situations requiring ethical decisions, including identifying conflicts of interest, recognizing and resolving ethical issues, etc. (Evaluate)2. Regulatory and legal issuesDescribe the importance of compliance to federal, national, and statutory regulations on software development. Determine the impact of issues such as copyright, intellectual property rights, product liability, and data privacy. (Understand) C. Standards and ModelsDefine and describe the ISO 9000 and IEEE software standards, and the SEI Capability Maturity Model Integration (CMMI) for development, services, and acquisition assessment models. (Understand)D. Leadership Skills1. Organizational leadershipUse leadership tools and techniques (e.g., organizational change management, knowledge transfer, motivation, mentoring and coaching, recognition). (Apply)2. Facilitation skillsUse facilitation and conflict resolution skills as well as negotiation techniques to manage and resolve issues. Use meeting management tools to maximize meeting effectiveness. (Apply)3. Communication skillsUse various communication methods in oral, written, and presentation formats. Use various techniques for working in multicultural environments, and identify and describe the impact that culture and communications can have on quality. (Apply)E. Team Skills1. Team managementUse various team management skills, including assigning roles and responsibilities, identifying the classic stages of team development (forming, storming, norming, performing, adjourning), monitoring and responding to group dynamics, working with diverse groups and in distributed work environments, and using techniques for working with virtual teams. (Apply)2. Team toolsUse decision-making and creativity tools such as brainstorming, nominal group technique (NGT), and multi-voting. (Apply)

II. Software Quality Management (22 questions)A. Quality Management System1. Quality goals and objectivesDesign software quality goals and objectives that are consistent with business objectives. Incorporate software quality goals and objectives into high-level program and project plans. Develop and use documents and processes necessary to support software quality management systems. (Create)2. Customers and other stakeholdersDescribe and analyze the effect of various stakeholder group requirements on software projects and products. (Analyze)3. OutsourcingDetermine the impact that outsourced services can have on organizational goals and objectives, and identify criteria for evaluating suppliers/vendors and subcontractors. (Analyze)4. Business continuity, data protection, and data managementDesign plans for business continuity, disaster recovery, business documentation and change management, information security, and protection of sensitive and personal data. (Analyze) B. Methodologies1. Cost of quality (COQ) and return on investment (ROI)Analyze COQ categories (prevention, appraisal, internal failure, external failure) and return on investment (ROI) metrics in relation to products and processes. (Analyze)2. Process improvement Define and describe elements of benchmarking, lean processes, the Six Sigma methodology, and use define, measure, act, improve, control (DMAIC) model and the plan-do-check-act (PDCA) model for process improvement. (Apply)3. Corrective action procedures Evaluate corrective action procedures related to software defects, process nonconformances, and other quality system deficiencies. (Evaluate)4. Defect prevention Design and use defect prevention processes such as technical reviews, software tools and technology, and special training. (Evaluate)C. Audits1. Audit typesDefine and distinguish between various audit types, including process, compliance, supplier, and system. (Understand)2. Audit roles and responsibilitiesIdentify roles and responsibilities for audit participants including client, lead auditor, audit team members, and auditee. (Understand)3. Audit processDefine and describe the steps in conducting an audit, developing and delivering an audit report, and determining appropriate follow-up activities. (Apply)III. System and Software Engineering Processes (32 questions)A. Life Cycles and Process Models1. Waterfall software development life cycleApply the waterfall life cycle and related process models, and identify their benefits and when they are used. (Apply)2. Incremental/iterative software development life cyclesApply the incremental and iterative life cycles and related process models, and identify their benefits and when they are used. (Apply)

Agile software development life cycleApply the agile life cycle and related process models, and identify their benefits and when they are used. (Apply)B. Systems ArchitectureIdentify and describe various architectures, including embedded systems, client-server, n-tier, web, wireless, messaging, and collaboration platforms, and analyze their impact on quality. (Analyze)C. Requirements Engineering1. Product requirements Define and describe various types of product requirements, including system, feature, function, interface, integration, performance, globalization, and localization. (Understand)2. Data/information requirements Define and describe various types of data and information requirements, including data management and data integrity. (Understand)3. Quality requirements Define and describe various types of quality requirements, including reliability and usability. (Understand)

4. Compliance requirementsDefine and describe various types of regulatory and safety requirements. (Understand)5. Security requirementsDefine and describe various types of security requirements including data security, information security, cybersecurity, and data privacy. (Understand)6. Requirements elicitation methodsDescribe and use various requirements elicitation methods, including customer needs analysis, use cases, human factors studies, usability prototypes, joint application development (JAD), storyboards, etc. (Apply)7. Requirements evaluationAssess the completeness, consistency, correctness, and testability of requirements, and determine their priority. (Evaluate)D. Requirements Management1. Requirements change managementAssess the impact that changes to requirements will have on software development processes for all types of life-cycle models. (Evaluate)2. Bidirectional traceabilityUse various tools and techniques to ensure bidirectional traceability from requirements elicitation and analysis through design and testing. (Apply)E. Software Analysis, Design, and Development1. Design methodsIdentify the steps used in software design and their functions, and define and distinguish between software design methods. (Understand)2. Quality attributes and designAnalyze the impact that quality-related elements (safety, security, reliability, usability, reusability, maintainability) can have on software design. (Analyze)3. Software reuseDefine and distinguish between software reuse, reengineering, and reverse engineering, and describe the impact these practices can have on software quality. (Understand)4. Software development toolsAnalyze and select the appropriate development tools for modeling, code analysis, requirements management, and documentation. (Analyze)F. Maintenance Management1. Maintenance typesDescribe the characteristics of corrective, adaptive, perfective, and preventive maintenance types. (Understand)2. Maintenance strategyDescribe various factors affecting the strategy for software maintenance, including service-level agreements (SLAs), short- and long-term costs, maintenance releases, and product discontinuance, and their impact on software quality. (Understand)3. Customer feedback managementDescribe the importance of customer feedback management including quality of product support and post-delivery issues analysis and resolution. (Understand)IV. Project Management (22 questions)A. Planning, Scheduling, and Deployment1. Project planningUse forecasts, resources, schedules, task and cost estimates, etc., to develop project plans. (Apply)2. Work breakdown structure (WBS) Use work breakdown structure (WBS) in scheduling and monitoring projects. (Apply)3. Project deploymentUse various tools, including milestones, objectives achieved, and task duration to set goals and deploy the project. (Apply)

B. Tracking and Controlling1. Phase transition controlUse various tools and techniques such as entry/exit criteria, quality gates, Gantt charts, integrated master schedules, etc., to control phase transitions. (Apply)2. Tracking methodsCalculate project-related costs, including earned value, deliverables, productivity, etc., and track the results against project baselines. (Apply)3. Project reviewsUse various types of project reviews such as phase-end, management, and retrospectives or post-project reviews to assess project performance and status, to review issues and risks, and to discover and capture lessons learned from the project. (Apply)4. Program reviewsDefine and describe various methods for reviewing and assessing programs in terms of their performance, technical accomplishments, resource utilization, etc. (Understand)C. Risk Management1. Risk management methodsUse risk management techniques (e.g., assess, prevent, mitigate, transfer) to evaluate project risks. (Evaluate)2. Software security risksEvaluate risks specific to software security, including deliberate attacks (hacking, sabotage, etc.), inherent defects that allow unauthorized access to data, and other security breaches. Plan appropriate responses to minimize their impact. (Evaluate)3. Safety and hazard analysisEvaluate safety risks and hazards related to software development and implementation and determine appropriate steps to minimize their impact. (Evaluate)V. Software Metrics and Analysis (19 questions)A. Process and Product Measurement1. Terminology Define and describe metric and measurement terms such as reliability, internal and external validity, explicit and derived measures, and variation. (Understand)2. Software product metricsChoose appropriate metrics to assess various software attributes (e.g., size, complexity, the amount of test coverage needed, requirements volatility, and overall system performance). (Apply)3. Software process metricsMeasure the effectiveness and efficiency of software processes (e.g., functional verification tests (FVT), cost, yield, customer impact, defect detection, defect containment, total defect containment effectiveness (TDCE), defect removal efficiency (DRE), process capability). (Apply)4. Data integrity Describe the importance of data integrity from planning through collection and analysis and apply various techniques to ensure data quality, accuracy, completeness, and timeliness. (Apply)B. Analysis and Reporting Techniques1. Metric reporting tools Using various metric representation tools, including dashboards, stoplight charts, etc., to report results. (Apply)2. Classic quality toolsDescribe the appropriate use of classic quality tools (e.g., flowcharts, Pareto charts, cause and effect diagrams, control charts, and histograms). (Apply)

3. Problem-solving toolsDescribe the appropriate use of problem solving tools (e.g., affinity and tree diagrams, matrix and activity network diagrams, root cause analysis and data flow diagrams [DFDs]). (Apply)VI. Software Verification and Validation (29 questions)A. Theory1. V&V methods Use software verification and validation methods (e.g., static analysis, structural analysis, mathematical proof, simulation, and automation) and determine which tasks should be iterated as a result of modifications. (Apply)2. Software product evaluationUse various evaluation methods on documentation, source code, etc., to determine whether user needs and project objectives have been satisfied. (Analyze)B. Test Planning and Design1. Test strategies Select and analyze test strategies (e.g., test-driven design, good-enough, risk-based, time-box, top-down, bottom-up, black-box, white-box, simulation, automation, etc.) for various situations. (Analyze) 2. Test plansDevelop and evaluate test plans and procedures, including system, acceptance, validation, etc., to determine whether project objectives are being met and risks are appropriately mitigated. (Create)3. Test designsSelect and evaluate various test designs, including fault insertion, fault-error handling, equivalence class partitioning, and boundary value. (Evaluate)4. Software testsIdentify and use various tests, including unit, functional, performance, integration, regression, usability, acceptance, certification, environmental load, stress, worst-case, perfective, exploratory, and system. (Apply)5. Tests of external products Determine appropriate levels of testing for integrating supplier, third-party, and subcontractor components and products. (Apply)6. Test coverage specificationsEvaluate the adequacy of test specifications such as functions, states, data and time domains, interfaces, security, and configurations that include internationalization and platform variances. (Evaluate)7. Code coverage techniquesUse and identify various tools and techniques to facilitate code coverage analysis techniques such as branch coverage, condition, domain, and boundary. (Apply)8. Test environmentsSelect and use simulations, test libraries, drivers, stubs, harnesses, etc., and identify parameters to establish a controlled test environment. (Analyze)9. Test toolsIdentify and use test utilities, diagnostics, automation, and test management tools. (Apply)10. Test data managementEnsure the integrity and security of test data through the use of configuration controls. (Apply)C. Reviews and InspectionsUse desk checks, peer reviews, walk-throughs, inspections, etc., to identify defects. (Apply)D. Test Execution DocumentsReview and evaluate test execution documents such as test results, defect reporting and tracking records, test completion metrics, trouble reports, and input/output specifications. (Evaluate)

VII. Software Configuration Management (20 questions)A. Configuration Infrastructure1. Configuration management teamDescribe the roles and responsibilities of a configuration management group. (Understand) (NOTE: The roles and responsibilities of the configuration control board [CCB] are covered in area VII.C.2.)2. Configuration management toolsDescribe configuration management tools as they are used for managing libraries, build systems, and defect tracking systems. (Understand)3. Library processes Describe dynamic, static, and controlled library processes and related procedures, such as check-in/check-out, and merge changes. (Understand)B. Configuration Identification 1. Configuration items Describe software configuration items (baselines, documentation, software code, equipment) and identification methods (naming conventions, versioning schemes). (Understand)2. Software builds and baselinesDescribe the relationship between software builds and baselines, and describe methods for controlling builds and baselines (automation, new versions). (Understand)C. Configuration Control and Status Accounting1. Item change and version controlDescribe processes for documentation control, item change tracking, version control that are used to manage various configurations, and describe processes used to manage configuration item dependencies in software builds and versioning. (Understand)2. Configuration control board (CCB)Describe the roles, responsibilities and processes of the CCB. (Understand) (NOTE: The roles and responsibilities of the configuration management team are covered in area VII.A.1.)3. Concurrent developmentDescribe the use of configuration management control principles in concurrent development processes. (Understand)4. Status accountingDiscuss various processes for establishing, maintaining, and reporting the status of configuration items, such as baselines, builds, and tools. (Understand)D. Configuration AuditsDefine and distinguish between functional and physical configuration audits and how they are used in relation to product specification. (Understand) E. Product Release and Distribution 1. Product releaseAssess the effectiveness of product release processes (planning, scheduling, defining hardware and software dependencies). (Evaluate)2. Customer deliverablesAssess the completeness of customer deliverables including packaged and hosted or downloadable products, license keys and user documentation, and marketing and training materials. (Evaluate)3. Archival processesAssess the effectiveness of source and release archival processes (backup planning and scheduling, data retrieval, archival of build environments, retention of historical records, offsite storage). (Evaluate)

Certified Software Quality Engineer Certification (CSQE)
Quality-Assurance Certification thinking
Killexams : Quality-Assurance Certification thinking - BingNews https://killexams.com/pass4sure/exam-detail/CSQE Search results Killexams : Quality-Assurance Certification thinking - BingNews https://killexams.com/pass4sure/exam-detail/CSQE https://killexams.com/exam_list/Quality-Assurance Killexams : Clarkson University's Course in Research Ethics Receives Quality Matters Certification for Course Design Quality

Clarkson University’s Research Ethics course earned the Quality Matters (QM) Certification Mark following a rigorous review process. The QM Certification Mark is the internationally recognized symbol of online and blended course design quality and represents Clarkson’s ongoing commitment to creating learning environments that provide learners with a clear pathway to success.

The certification is the result of Clarkson’s dedication to continuous improvement, including the professional direction by Senior Instructional Designer Loretta Driskel and Course Instructors. BIE 555 Research Ethics I is the first Clarkson University course to achieve certification in 2023 and is listed on the QM directory of certified courses.

BIE 555 is part of the Caribbean Research Ethics Education Initiative (CREEii), which is funded by a National Institutes of Health Fogarty International Center (NIH FIC) grant. The funding aims to build research ethics capacity in the English- and Spanish-speaking Caribbean basin and provides a MS Bioethics degree education at Clarkson University to three cohorts of 15 CREEii fellows. 

The cohorts of fellows are mixed language - Spanish and English, with some bilingual, some of limited English proficiency, and some monolingual. This course has a Spanish-language and an English-language faculty member, who share teaching responsibilities while teaching in their native language. The course uses artificial intelligence translation from Google to allow web pages to be automatically translated into whatever language the user - faculty or student - wishes. 

Reading assignments are translated using the Google translate site and made available to students or, when not possible, equivalent content is made available from native language texts. The design of the curriculum to incorporate simultaneous bilingual instruction is intended to allow for the development of courses that are responsive to the unique research ethics needs of the Caribbean basin countries while fostering cross-cultural understanding and relationships.

Clarkson’s institutional participation in Quality Matters is vital to achieving adherence to online learning quality standards. By encouraging courses to meet quality standards, Clarkson is making important strides to keep pace with a third of other institutions. Nearly all other institutions require all or at least some of their online courses to meet quality assurance standards according to CHLOE 2021, a survey of chief online officers (Garrett 2021). Instructors who are interested in pursuing QM certification for their online or blended learning course are encouraged to contact the Clarkson’s Teaching & Learning Corner at tlc@clarkson.edu to learn more.

Clarkson University has been recognized by Quality Matters for the following courses:

  • BIE555 - Research Ethics, Sharmella R Martin Bernardo Garcia Camino Feb 02, 2023

  • OM680 Strategic Project Management, Michael Bissonette Dec 12, 2022

  • OM650 Operations Strategy and International Competitiveness, Jon Brink Oct 18, 2022

  • ED571 Middle Adolescence Literacy, Judy Morley Apr 20, 2022

  • TE540 Foundations of Teaching TESOL, Karen Gregory & Gretchen Oliver Feb 17, 2022

  • BIE573 Interpersonal Skills and Communication, Ellen Tobin Ballato Dec 08, 2021

  • ED573 Virtual Learning in the P-12 Classroom, Erin Blauvelt Mar 12, 2021

  • EE603/ME578/BOE620 Statistical Methods for Reliability and Life Data Analysis, Daniel Eno Dec 03, 2020

  • OM603 Decision Analysis & Supply Chain Modeling, William MacKinnon Mar 19, 2020

  • BIE 577 Managerial Epidemiology - Managerial Epidemiology, Jane Oppenlander May 03, 2019

  • EM680 Decision Analysis and Risk Management, William MacKinnon Oct 26, 2018

  • HC602 Advanced Statistics and Data Visualization, Jane Oppenlander Jun 22, 2018

Clarkson University uses the Quality Matters Rubric as a guideline in all course development and revision. The QM Rubric and process fit perfectly into our mission of providing quality online courses to students.

Grounded in research. Driven by best practices. A community that puts learners first. Quality Matters (QM) is the global organization leading quality assurance in online and innovative digital teaching and learning environments. It provides a scalable quality assurance system for online and blended learning used within and across organizations. When you see QM Certification Marks on courses or programs, it means they have met QM Course Design Standards or QM Program Review Criteria in a rigorous review process.

Thu, 09 Feb 2023 04:54:00 -0600 en text/html https://www.clarkson.edu/news/clarkson-universitys-course-research-ethics-receives-quality-matters-certification-course
Killexams : McLeod Health Certified to ISO 9001 Quality Management System by DNV

Florence, SC - McLeod Health has been awarded full certification to the ISO 9001 Quality Management System by DNV.

“McLeod Health is dedicated to providing the safest and most effective healthcare services possible,” said Madge Hamer, Associate Vice President of Accreditation and Certification for McLeod. “ISO 9001 certification not only reflects that mission but helps to empower it. The effort required to achieve this certification fundamentally transforms the way we do business – it gets everyone on the same page and helps us achieve our objectives.”

ISO 9001 is the most widely accepted quality management system in use around the world and is quickly gaining acceptance among U.S. healthcare providers as a foundation for their quality and patient safety programs.

“McLeod Health has worked hard to achieve this certification, and they have done so with unwavering commitment from their top leadership to make their organization the best it can be,” said Kelly Proctor, President of DNV Healthcare USA Inc. “ISO 9001 certification isn’t just an award or trophy for something you’ve done, it’s public evidence that you are at the top of your game with an obvious plan in place to make excellence an every day objective.”

ISO 9001 brings science to the art of caregiving; it helps to standardize processes around things that are proven to work, by the people doing the work, thus empowering frontline workers while creating an environment of predictability for the entire organization. The ultimate impact of ISO 9001 within hospitals is the reduction or elimination of variation, so that critical work processes are done consistently, and the “best ideas” aren’t held by one person or one department but are ingrained in the organization itself.

Businesses that implement ISO 9001 do so for both the internal and external benefits. Internally it helps staff create clear and consistent processes of patient care and ensure that progress is constantly being made toward specific quality objectives. Externally, it tells the public, as well as insurers and regulatory agencies, that the hospital is not only talking about quality, but is pursuing it with discipline and transparency.

About McLeod Health

Founded in 1906, McLeod Health is a locally owned and managed, not for profit organization supported by the strength of more than 900 members on its medical staff and more than 2,900 licensed nurses (Registered Nurses; Advanced Practice Nurses – including Certified Nurse Anesthetists, Nurse Practitioners and Certified Nurse Midwives; as well as Licensed Practical Nurses). McLeod Health is also composed of approximately 15,000 team members and more than 90 physician practices throughout its 18-county service area. With seven hospitals, McLeod Health operates three Health and Fitness Centers, a Sports Medicine and Outpatient Rehabilitation Center, Hospice and Home Health Services. The system currently has 988 licensed beds, including Hospice and Behavioral Health. The hospitals within McLeod Health include: McLeod Regional Medical Center, McLeod Health Dillon, McLeod Health Loris, McLeod Health Seacoast, McLeod Health Cheraw, McLeod Health Clarendon and McLeod Behavioral Health. On the coast, the McLeod Health Carolina Forest complex has an Emergency Department and the first two of seven medical park office buildings as an extension of McLeod Loris Seacoast Hospital. Projected to open in spring 2023, Building 3 on the McLeod Health Carolina Forest Campus will include the following services and medical specialties: orthopedics, rehabilitation, obstetrics and gynecology, pulmonary and critical care, rheumatology, general surgery and digestive health.

About DNV

DNV is a global independent certification, assurance and risk management provider, operating in more than 100 countries. Through its broad experience and deep expertise, DNV advances safety and sustainable performance, sets industry benchmarks, drives innovative solutions.

Whether certifying a company’s management system or products, accrediting hospitals, providing training, assessing supply chains or digital assets, DNV enables customers and stakeholders to make critical decisions with confidence, continually Boost and realize long-term strategic goals sustainably.

DNV draws on its wide technical and industry expertise to help companies worldwide build consumer and stakeholder trust. Driven by its purpose, to safeguard life, property, and the environment, DNV helps tackle the challenges and global transformations facing its customers and the world today and is a trusted voice for many of the world’s most successful and forward-thinking companies.

For more information about DNV, please visit www.dnvcert.com/healthcare.

Mon, 13 Feb 2023 03:32:00 -0600 en text/html https://www.postandcourier.com/kingstree/community-news/mcleod-health-certified-to-iso-9001-quality-management-system-by-dnv/article_28e315d0-a8a8-11ed-9169-d3f6dac51956.html
Killexams : Beef Quality Assurance and Transportation certification offered

Beef producers and transporters have several opportunities to receive or renew their Beef Quality Assurance and Beef Quality Assurance Transportation certification in March. The dates and locations of trainings in southwest Nebraska are:

Imperial: 4 p.m. MT March 6, Crossroads Wesleyan Church, 220 W. 17th St.

Holdrege: 4 p.m. CT March 7, Phelps County Ag Center, 1308 Second St.

North Platte: 4 p.m. Ct March 8, West Central Research Extension and Education Center, 402 W. State Farm Road.

The certification trainings are provided by Nebraska Beef Quality Assurance, a program of University of Nebraska-Lincoln Extension.

Many commercial beef packing facilities require producers who sell fed cattle to them to be BQA certified and those who deliver cattle to their facilities to be BQAT certified.

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The certifications are valid for three years.

Topics addressed at the trainings include:

Animal health best management practices.

Proper animal welfare guidelines.

“Beef cattle producers who are committed to producing quality, wholesome and safe beef and beef products for consumers are encouraged to attend to stay up to date on BQA practices,” said Jesse Fulton, director of Nebraska Beef Quality Assurance.

“By becoming or staying BQA and BQAT certified you are an integral part of beef’s positive story to consumers — a story that can increase their understanding and confidence in how you and your operation are raising and transporting an animal that is fit to enter the beef supply chain,” Fulton said.

The certification fee is $20 per person or a flat fee of $100 for operations that bring five or more people.

Attendees must pre-register online at bqa.unl.edu or by calling the UNL Panhandle Research Extension and Education Center at 308-632-1230. Locations with no one registered will be canceled.

Those who call in their registrations will need to supply names and phone numbers for all those registering. Additionally, an email address will need to be provided for certificates to be electronically issued.

For all other inquiries, contact Nebraska BQA via email at nebraskabqa@unl.edu or by phone at 308-633-0158.

Sat, 11 Feb 2023 15:31:00 -0600 en text/html https://nptelegraph.com/lifestyles/beef-quality-assurance-and-transportation-certification-offered/article_19b870b2-a891-11ed-9596-abbef13986c3.html
Killexams : Software Quality Assurance (SQA) Testing Market Size 2023 Will Touch A New Level In The Upcoming Year 2029

The MarketWatch News Department was not involved in the creation of this content.

Feb 14, 2023 (The Expresswire) -- Pre and Post Covid Report Is Covered | Final Report Will Add the Analysis of the Impact of Russia-Ukraine War and COVID-19 on This Industry.

[124 Pages Report]"Software Quality Assurance (SQA) Testing Market" size is projected to reach Multimillion USD by 2029, In comparison to 2023, at unexpected CAGR during 2023-2029 and generated magnificent revenue. This study provides all the most exact market facts and trends for your business analytics and strategic decision-making. This Software Quality Assurance (SQA) Testing Market research report is meant to be helpful to all business owners, investors, and stakeholders in the industry. It provides significant insights into the factors affecting the global Software Quality Assurance (SQA) Testing market and the industry's yearly growth.

The market is segmented on the basis of End-user Industry (Artificial Intelligence Testing, Cybersecurity Testing, Blockchain Testing, IoT Testing, Others), By Type (Test Consulting And Compliance, Quality Assurance Testing, Application And Software Testing, Risk And Compliance Testing Covering, Others), and Geography (Asia-Pacific, North America, Europe, South America, and Middle-East and Africa).

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GlobalSoftware Quality Assurance (SQA) Testing MarketReport 2023 is spread across124 pagesand provides exclusive vital statistics, data, information, trends and competitive landscape insights in this niche sector.

Who are some of the key players operating in the Software Quality Assurance (SQA) Testing market and how high is the competition 2023?

Company Information: List by Country Top Manufacturers/ Key Players In Software Quality Assurance (SQA) Testing Market Insights Report Are:

● TestPlant eggPlant Functional ● TCS ● Tricentis Tosca Testsuite ● Worksoft Certify ● IBM ● Cognizant ● HP ● Katalon Studio ● Capgemini ● Wipro ● Infosys ● Hexaware

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The Global Software Quality Assurance (SQA) Testing market is anticipated to rise at a considerable rate during the forecast period, between 2023 and 2029. In 2022, the market is growing at a steady rate and with the rising adoption of strategies by key players, the market is expected to rise over the projected horizon.

According to this latest study, the 2023 development of Third-Party Replacement Strap for Software Quality Assurance (SQA) Testing will have huge change from earlier year.

Software Quality Assurance (SQA) Testing Market size, segment (mainly covering Major Type (Test Consulting And Compliance, Quality Assurance Testing, Application And Software Testing, Risk And Compliance Testing Covering, Others), End Users (Artificial Intelligence Testing, Cybersecurity Testing, Blockchain Testing, IoT Testing, Others), and regions), exact status, development trendsa and competitor landscape. Furthermore, the 124 pages report provides detailed cost analysis, supply chain.

Technological innovation and advancement will further optimize the performance of the product, making it more widely used in downstream end users. Also, Consumer behaviour analysis and market dynamics (drivers, restraints, opportunities) provides crucial information for knowing the Software Quality Assurance (SQA) Testing market.

Software Quality Assurance (SQA) Testing market identifies the increase in RandD of therapeutic vaccines as one of the prime reasons driving the Software Quality Assurance (SQA) Testing Market growth during the next few years. Also, increased disease diagnostic modalities, and increasing research on combination therapies will lead to sizable demand in the market.

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It also discussions about the market size of different segments and their growth aspects along with Competitive benchmarking, Historical data and forecasts, Company revenue shares, Regional opportunities, Latest trends and dynamics, growth trends, various stakeholders like investors, CEOs, traders, suppliers, Research and media, Global Manager, Director, President, SWOT analysis i.e. Strength, Weakness, Opportunities and Threat to the organization and others. Revenue forecast, company share, competitive landscape, growth factors and trends

What are the major applications and type, of Software Quality Assurance (SQA) Testing?

Major Product Types of Software Quality Assurance (SQA) Testing covered are:

● Test Consulting And Compliance ● Quality Assurance Testing ● Application And Software Testing ● Risk And Compliance Testing Covering ● Others

Major Applications of Software Quality Assurance (SQA) Testing covered are:

● Artificial Intelligence Testing ● Cybersecurity Testing ● Blockchain Testing ● IoT Testing ● Others

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Market Growth Reports present a detailed picture of the market by the way of study, and summation of data from multiple sources by an analysis of key parameters. Our antimicrobial therapeutics market covers the following areas:

● Software Quality Assurance (SQA) Testing market sizing ● Software Quality Assurance (SQA) Testing market forecasts ● Software Quality Assurance (SQA) Testing market industry analysis

What is our report scope?

This report focuses on the Software Quality Assurance (SQA) Testing in Global market, especially in North America, Europe and Asia-Pacific, South America, Middle East and Africa. This report categorizes the market based on manufacturers, regions, type and application. The Software Quality Assurance (SQA) Testing-market report gives the clear picture of current market scenario which includes historical and projected market size in terms of value and volume, technological advancement, macro economical and governing factors in the market.

What are the major regional markets of Software Quality Assurance (SQA) Testing in Global, according to the Market Growth Reports report?

Software Quality Assurance (SQA) Testing Market analysis, by Geography: Major regions covered within the report: Consumption by Region 2023: -

● North America (U.S. and Canada) Market size, Software Quality Assurance (SQA) Testing growth, Market Players Analysis and Opportunity Outlook ● Latin America (Brazil, Mexico, Argentina, Rest of Latin America) Market size, Software Quality Assurance (SQA) Testing growth and Market Players Analysis and Opportunity Outlook ● Europe (U.K., Germany, France, Italy, Spain, Hungary, Belgium, Netherlands and Luxembourg, NORDIC (Finland, Sweden, Norway, Denmark), Ireland, Switzerland, Austria, Poland, Turkey, Russia, Rest of Europe), Poland, Turkey, Russia, Rest of Europe) Market size, Software Quality Assurance (SQA) Testing growth Market Players Analyst and Opportunity Outlook ● Asia-Pacific (China, India, Japan, South Korea, Singapore, Indonesia, Malaysia, Australia, New Zealand, Rest of Asia-Pacific) Market size, Software Quality Assurance (SQA) Testing growth and Market Players Analysis and Opportunity Outlook ● Middle East and Africa (Israel, GCC (Saudi Arabia, UAE, Bahrain, Kuwait, Qatar, Oman), North Africa, South Africa, Rest of Middle East and Africa) Market size, Software Quality Assurance (SQA) Testing growth Market Players Analysis and Opportunity Outlook

The report can help to know the market and strategize for business expansion accordingly. Within the strategy analysis, it gives insights from market positioning and marketing channel to potential growth strategies, providing in-depth analysis for brand fresh entrants or exists competitors within the Software Quality Assurance (SQA) Testing industry. Global Software Quality Assurance (SQA) Testing Market Report 2023 provides exclusive statistics, data, information, trends and competitive landscape details during this niche sector.

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With tables and figures helping analyze worldwide Global Software Quality Assurance (SQA) Testing Market Forecast this research provides key statistics on the state of the industry and should be a valuable source of guidance and direction for companies and individuals interested in the market.

Major Points from Table of Contents:

Global Software Quality Assurance (SQA) Testing Market Research Report 2023-2029, by Manufacturers, Regions, Types and Applications

1 Introduction
1.1 Objective of the Study
1.2 Definition of the Market
1.3 Market Scope
1.3.1 Market Segment by Type, Application and Marketing Channel
1.3.2 Major Regions Covered (North America, Europe, Asia Pacific, Mid East and Africa)
1.4 Years Considered for the Study (2017-2029)
1.5 Currency Considered (U.S. Dollar)
1.6 Stakeholders

2 Key Findings of the Study

3 Market Dynamics
3.1 Driving Factors for this Market
3.2 Factors Challenging the Market
3.3 Opportunities of the Global Software Quality Assurance (SQA) Testing Market (Regions, Growing/Emerging Downstream Market Analysis)
3.4 Technological and Market Developments in the Software Quality Assurance (SQA) Testing Market
3.5 Industry News by Region
3.6 Regulatory Scenario by Region/Country
3.7 Market Investment Scenario Strategic Recommendations Analysis

4 Value Chain of the Software Quality Assurance (SQA) Testing Market

4.1 Value Chain Status
4.2 Upstream Raw Material Analysis
4.3 Midstream Major Company Analysis (by Manufacturing Base, by Product Type)
4.4 Distributors/Traders
4.5 Downstream Major Customer Analysis (by Region)

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5 Global Software Quality Assurance (SQA) Testing Market-Segmentation by Type
6 Global Software Quality Assurance (SQA) Testing Market-Segmentation by Application

7 Global Software Quality Assurance (SQA) Testing Market-Segmentation by Marketing Channel
7.1 Traditional Marketing Channel (Offline)
7.2 Online Channel

8 Competitive Intelligence Company Profiles

9 Global Software Quality Assurance (SQA) Testing Market-Segmentation by Geography

9.1 North America
9.2 Europe
9.3 Asia-Pacific
9.4 Latin America

9.5 Middle East and Africa

10 Future Forecast of the Global Software Quality Assurance (SQA) Testing Market from 2023-2029

10.1 Future Forecast of the Global Software Quality Assurance (SQA) Testing Market from 2023-2029 Segment by Region
10.2 Global Software Quality Assurance (SQA) Testing Production and Growth Rate Forecast by Type (2023-2029)
10.3 Global Software Quality Assurance (SQA) Testing Consumption and Growth Rate Forecast by Application (2023-2029)

11 Appendix
11.1 Methodology
12.2 Research Data Source

Continued….

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Reasons to buy this report:

● To get a comprehensive overview of the Software Quality Assurance (SQA) Testing Market ● To gain wide ranging information about the top players in this industry, their product portfolios, and key strategies adopted by the players. ● To gain insights of the countries/regions in the Software Quality Assurance (SQA) Testing Market.

Customization of the Report

Our research analysts will help you to get customized details for your report, which can be modified in terms of a specific region, application or any statistical details. In addition, we are always willing to comply with the study, which triangulated with your own data to make the market research more comprehensive in your perspective.

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Killexams : EXCLUSIVE: How To Lower The Cost Of Cannabis Quality And Save 30% Of Your Top-Line Revenue

Cannabis companies of all sizes are struggling to increase their profit margins and to make that happen, they're implementing different strategies. Lowering prices and premiumizing products are among the alternatives to create value. In addition, cannabis companies might look at risk mitigation as an alternative to achieve higher quality and prevent losses.

How can cannabis companies ensure higher quality with a sustainable ROI? Or, how cannabis companies can achieve premiumization at a lower cost?

A quality management system (QMS) might help. QMS are popular in many industries. Automobiles, planes, medical devices and cannabis companies are no different when it comes to quality assurance. Likewise, electronic QMS are software tools that offer cannabis companies an automated means to record and manage all business-critical information, mitigate risk, ensure quality standards and comply with a myriad of regulations.

Good Costs, Poor Costs

The cannabis industry can be viewed as an amalgamation of regulatory elements of pharma, agriculture, consumer packaged goods, food and beverage. However, there are nuances. Regulations can take many shapes and “that's where companies like C15 come in,” Sean Samuel, VP of Sales and Marketing told Benzinga in an exclusive interview. 

C15 delivers a life sciences-based electronic Quality Management System platform to raise quality, compliance and safety standards. 

“We are considered a risk mitigation tool. We're solving the cost of quality which it's not the cost of goods sold. Typically will not show up on a P&L statement. However, these are massive costs that typically represent anywhere between 25 to 35% of your top-line revenue. The cost of quality can be broken down into good costs and bad costs,” Samuel said.

“The good costs are things like, a risk management procedure, validation, internal audits, table stakes when it comes to quality management. The poor costs are where the cost of quality can skyrocket. Any time a batch doesn't get released because there's been mold contamination. Costs that aren't tangible to a lot of C-suites in the cannabis space.”

Disaster Prevention

According to Samuel, good costs can be seen as an opportunity. Any time there are customer returns, complaints, there's damage to the brand reputation, these are foregone sales that companies could have had. Without mentioning a recall. That can be an absolute disaster.

While executives from cannabis companies spend hours thinking about how to create value for stakeholders, a 2-micron mold spore can destroy everything in one harvest.

Samuel explained that resorting to a system such as C15’s can significantly decrease the chances of unfortunate events like that. For a graphic description, he provided an example.

“The sixth largest licensed producer in Canada lost their license because they were doing non-compliant things and they had very poor record-keeping. They got delisted from the Toronto Stock Exchange,” Samuel said. “We are talking shareholder value destruction to the tune of like tens of millions, all because of record keeping. It's not a cost that you can just reduce your expenses on. If not managed properly, the cost of quality can represent millions,” Samuel added, referring to quality management, as a “core task to kill a mess.”

Integrate Everything

From inventory, which is typically what an enterprise resource planning system (ERP) would address, to environmental controls, C15 can monitor and evaluate everything.

Over 300 open applications enable software to communicate to cover the entire supply chain and ensure that protocols and regulations are met.

“Our system comes preloaded with validated audit workflows for supplier qualification, external audits, and internal audits. When the supplier is approved, the system sends a message to the production team, so they know they can purchase from them,’” Samuel said. “You can put that supplier on hold.”

"Our system is effectively the blueprint for production as well as the remedial actions for when things go wrong in the production process. We connect the whole facility.” 

Proven Efficiency

To expand to international markets, C15 has gone through the EU GMP validation process from top to bottom. The company has customers in eight different countries, including New Zealand, Australia and Uruguay. And some of them are in emerging international EU GMP markets, such as the United Kingdom.

In addition, the firm partnered with publicly-traded $25 billion company Veeva Systems Inc. VEEV, operating in the biotech sector. Bayer BAYRY, Pfizer PFE, Merck & Co. MRK, GSK GSK, Unilever plc UL, and Kraft Heinz KHC are among its clientele.

Samuel noted that global cannabis companies, MSOs, and larger single-state operators are gravitating towards C15 seeking an alternative to navigating different regulations, with one single software system.

And provided an example of how C15 is currently working with cannabis MSO Curaleaf CURLF.

“Through our system, Curaleaf harmonizes certain processes and procedures across its national footprint while customizing others. We can tailor document approval workflows for different states. Employees can see certain SOPs, and training material, whereas the C-suite can see everything across the operation,” Samuel explained.

Training and Retail

Cannabis companies can have anywhere between 500 to 1000 Standard Operational Procedures and they might make revisions to half of them over an annual basis. Every time companies make changes to an SOP, they need to retrain the impacted staff so they know they're using the latest and greatest procedures. And that's a ton of training.

Thus, C15 evolved its training above and beyond just SOP compliance training, and it now comes with what Samuel calls “a full-blown training management solution” that allows companies to develop a role-based curriculum.

“You may have a generic curriculum that deploys that applies to all employees, and then a role-specific curriculum that can be any training requirements you want. Training requirements could be SOPs, they could be videos, they could be PowerPoint scoring files, quite literally, anything. We've rolled out this training solution that trickles down, from production to retail stores,” Samuel said.

‘J.D. Power, have you heard of that?’

“We aggregate a lot of production data, deviation data, complaint data… that is kind of like the next chapter of our company, we're very much looking at how to market this data.

“We're providing our customers with annual report cards. So based on an anonymous aggregate customer curve, looking at all our customer data, and how they can be leveraging the system,” Samuel continued.

“J.D. Power, have you heard of that? They offer a sort of quality curve for the automotive industry. J.D. survey customers and tell automobile companies how they sit on the broader quality curve. We're going to tell customers, here's where you can use the system. Here's where you're underutilizing the system,” Samuel concluded.

Photo: Janon Stock on Shutterstock, photo Courtesy of Sean Samuel VP Sales & Marketing - C15 Solutions, Inc.

© 2023 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

Wed, 15 Feb 2023 02:50:00 -0600 en text/html https://www.benzinga.com/general/biotech/23/02/30915385/exclusive-how-to-lower-the-cost-of-cannabis-quality-and-save-30-of-your-top-line-revenue
Killexams : Best Delta 9 Gummies: Top 4 THC Edibles Of 2023

Delta 9 gummies are a tasty way to consume THC. They are strong and excellent for reducing stress.

However, a cannabinoid is used by individuals for a variety of purposes in addition to promoting relaxation. You could want to use it, for instance, to get more rest, feel less anxious, or get some pain relief.

The gummies offer a delectable, tranquil way to unwind and refocus naturally. Additionally, the delta-9 THC is generated from hemp, making it acceptable under the 2018 Farm Bill.

Delta-9 has been a widely used medication for many years. Due to this delivery mechanism's discrete and recognizable character, it is usually consumed in gummy form.

In addition, if you haven't heard, buying Delta 9 gummies online, along with CBD and other retail hemp goods, is now acceptable.

However, choosing a brand from the wide range of possibilities on the market may sometimes be challenging. Consequently, we have researched and gathered information about the top brands of Delta 9 gummies on the market.

Let's examine these top delta 9 gummies and see what makes them special. Both the tastes and the way the gummies leave you feeling will be to your liking. Let's start now.

Our Picks For The Best Delta 9 Gummies (Reviewed)

Exhale Wellness - Overall Best Delta 9 Gummies On The Market

BudPop - Strongest Delta 9 THC Gummies With Variety Of Flavors

Cheef Botanicals - Highly Potent Delta 9 Edibles; Non GMO

Delta Extrax - Vegan Delta 9 Gummies Infused With THC

#1. Exhale Wellness - Overall Best Delta 9 Gummies On The Market

Exhale Wellness
Exhale Wellness

Even though they have been selling high-quality Delta-8 items for quite some time, Exhale Wellness has just recently expanded its selection to include Delta-9 varieties. They are a well-known LA firm that uses only sustainable materials.

For this reason, we can confidently endorse Exhale Wellness products. Locating a hemp-focused vendor is your best chance if you're on the hunt for the best Delta 9 gummies.

Colorado is one of the most well-known states for organic hemp production, and here is where the hemp used in Exhale products is from. Also, the full-spectrum hemp used in the final goods is organic and non-GMO, which helps establish the legitimacy of the brand.

Features

Powerful: These candies are available in either 750 mg or 1500 mg strength. Every pack of candies in the 750mg bottle contains 30 milligrams of THC, for a total of 1 milligrams of THC per candy. In addition, each treat has 2 milligrams of gummies for 60 milligrams in each box.

Beneficial to health: As an added bonus to its health benefits, the creators of delta 9 gummies recently uncovered a tasty and effective method to help you recover from your physical ailments.

One possible benefit of these gummies is improved focus and productivity throughout the day, but they may also help with other health issues.

For example, assist you in dealing with stress by facilitating restful sleep at night. They are highly concentrated and effective immediately; therefore, new customers should follow the guidelines laid forth on the firm's site.

Analysis: Do all these gummies leave you with any doubts about the analysis? Check the certificate of analysis for more information on the excellence of these treats.

As an added measure, each item undergoes independent safety and purity testing. Because of this, you can be certain that these snacks are completely free of any potentially dangerous chemicals.

Natural: The hemp used to manufacture these gummies is grown organically in Colorado. Similarly, they are made without the use of any synthetic ingredients or gluten and instead use only natural and organic materials. In addition, the candies' vibrant hue comes from the use of real fruit juice in their production.

Pros

  • Aspects of using natural treatments
  • Lacking artificial flavors and hues
  • A choice between two sizes
  • The fruity flavors are just delicious.
  • An easy packing method
  • Personally researched
  • Free shipping and handling

Cons

  • Its strength might be overwhelming for novices.

Customers' Reviews

Customers report feeling instantly calmer after consuming these Delta 9 gummies, much to the delight of the company. In addition, customers supply Good Marks to the product because they like the taste and the easy chewing smoothness.

=> Click here to visit the official website “Exhale Wellness”

#2. BudPop - Strongest Delta 9 THC Gummies With Variety Of Flavors

BudPop
BudPop

BudPop has made a name for itself as a reliable source for high-quality Delta-8 goods, and they've now moved into the Delta-9 market. We're comfortable recommending BudPop since we know they put a premium on quality.

When on the lookout for D9 gummies, it's imperative that you first look for hemp as a basis. BudPop sources its hemp from Colorado, a place well recognized for its high-quality hemp harvest. Plus, the products use non-GMO and natural full-spectrum hemp, adding to the reliability of the brand.

Features

Extremely stringent standards: BudPop's products regularly undergo extensive testing at an independent lab to ensure their superior quality. They are chemical & metal-free, cruelty-free, and suitable for vegans. Only hemp grown on farms licensed by the USDA is used in BudPop products.

All products are hemp-based with a THC concentration of less than 0.3 percent, as the Farm Bill requires. There is 7.5mg of Delta 9 in each package of BudPop's Delta 9 gummies, plus 1 mg of other cannabinoids. CO2 extraction methods are used by the firm as well, which is standard practice for the industry.

Operation: Legislation is reasonable, and the prices of this brand's products are low. BudPop collaborates with charitable organizations and gives back a portion of its proceeds.

There isn't a minimum order size, and the free shipping is a huge perk. In addition, the organization provides standard and fast shipping options. Finally, a 30-day money-back policy with a 2-week time restriction is offered by BudPop.

Safe and sound: BudPop only deals with a trusted payment processor. Due to the prevalence of online fraudsters, many customers are wary about using their credit cards to make purchases. BudPop has your back by encrypting all of your information for maximum security.

Some hemp consumers feel the same way about their personal information. Maybe it's because the whole delta 9 industry is still frowned upon by the general public. You may be certain that you will have the privacy you want while purchasing from BudPop.

Flavor: There are other delta 9 gummy tastes, like Watermelon Zkittlez and Strawberry Gelato, that are just as delicious as Blue Dream Berry.

The gummy bears with strawberry taste combine the Indica dominating strain with the sweet fruitiness. Watermelon Zkittlez also contains the popular Zkittles strain, which helps increase focus while also relaxing sore muscles.

Pros

  • Safe, Farm Act-compliant hemp cultivated in the United States
  • Certificates of analysis(COA) are available and may be verified.
  • The website that prioritizes its visitors
  • Guaranteed refund within 30 days
  • Free shipping and handling
  • You'll get 20 percent off your first transaction.

Cons

  • Only available through the World Wide Web

Customers' Reviews

Because the Delta 9 series is so recent, there are few reviews from genuine customers just yet. On the other hand, BudPop's other products have received overwhelmingly positive feedback from customers.

Many buyers have commented on how comfortable they feel shopping here and how high-quality everything is. Consumers also liked BudPop products since they worked quickly to provide the intended effect.

In addition to our positive experience, we appreciated the company's generous 30-day return policy and free shipping on all orders. As a result, we know their Delta 9 gummies will be just as good as ours.

=> Click here to visit the official website “BudPop”

#3. Cheef Botanicals - Highly Potent Delta 9 Edibles; Non GMO

Cheef Botanicals
Cheef Botanicals

This company has been in business for more than five years. Additionally, it is among the greatest locations to get the ideal size and strength of delta 9 gummies.

You can get premium, delta 9 gummies from Cheef Botanicals without a prescription. Aside from that, this business makes gummies in two flavors: watermelon as well as blue raspberry.

Furthermore, Cheef Botanicals gummies include strong, premium compounds that provide customers immediate pain and stress relief.

Also, these delta 9 gummies' potent organic ingredients and lengthy intake intervals enable consumers to safely trigger neurodegeneration.

As a result, you may enhance both your general mental and physical well-being and the amount of sleep. Additionally, Cheef Botanicals provides a range of CBD goods, including full-spectrum CBD oils.

Highlights

Trusted Product: Cheef Botanicals has been in business for more than five years and has a history of delivering top-notch goods. Also, this company has over 5000 favorable evaluations, demonstrating that buyers are happy with their goods.

Additionally, only hemp flowers sourced from the greatest hemp-growing states, such as Colorado, Washington, and Oregon, are used by this business. Additionally, the THC content of these gummies is less than 0.3%, which is below the legal limit.

30-Day Cash-Refund Policy: Returning items to this brand is hassle-free, which is another advantage. Although this company offers premium gummies, not all customers will be happy with their purchases.

Therefore, if you're dissatisfied with your purchase, this brand lets you ask for a refund. Please note that this promotion is only valid for 30 days after your purchase receipt.

Vegan-Friendly: We appreciate this firm since they place a high value on using natural products. This company makes secure, vegan-friendly gummies.

Additionally, they are free of GMOs, synthetic flavors, preservatives, and other harmful ingredients. So, when you partake in these gummies, you don't need to be concerned about any adverse effects.

Top-notch Customer Service: According to Cheef Botanicals, their customer service is among the finest in the hemp sector. This company has a helpful and accommodating customer support crew that is prepared to address any problem you may have.

Moreover, every complaint you make is resolved in 24 hours. You may contact the customer support department through email or e-chat messenger on their official website.

Resources for Education: In addition to offering high-quality goods, this company is committed to teaching its clients about the various advantages of plant dietary supplements.

Their publications, however, primarily highlight the health advantages of THC as well as other cannabinoids present in the hemp plant. Therefore, if you want to understand more about the hemp plant, visit their official website.

Pros

  • Exceptional client service.
  • Get a full refund if you're not satisfied with our services within 30 days.
  • The 2018 Farm Bill codifies the legality of full-spectrum hemp extract oil.
  • Ingredients derived only from hemp plants and not animals

Cons

  • The previous one has been replaced with a second option.

Customers’ Reviews

The gummies get overwhelmingly positive reviews on the manufacturer's website. Happy consumers have lauded both the shipping speed and the return policies.

In addition, the great majority of purchasers have noted that the gummies assisted them in getting a good night's rest.

Finally, clients express fervent enthusiasm for the candies among friends and family after trying them and praising their great quality and wonderful natural flavors.

=> Click here to visit the official website “Cheef Botanicals”

#4. Delta Extrax - Vegan Delta 9 Gummies Infused With THC

 Cheef Botanicals
 Delta Extrax

Delta Extrax provides a broad selection of products so that all of their hemp-loving consumers may discover something that meets their needs. Their whole Delta 9 product range is both risk-free and designed to amaze, so everybody, from seasoned experts to first-time consumers, may benefit.

Due to its commitment to keeping up with the latest changes in the business and creating more helpful goods and services, the firm has established a strong reputation in the marketplace.

They advertise the concept that we can cure a wide variety of ailments with natural treatments and provide products to support this claim.

Therefore, you may learn more about the benefits of delta 9 products as well as the best methods to incorporate them into your lifestyle.

Delta Extrax only uses the highest quality Sativa and Indica strains and adheres to strict environmental guidelines to produce their products.

Features

Effective: Delta Extrax is now a household name in the delta 9 market because of its potent composition and dedication to sustainable cultivation and the use of exclusively organic components.

The producer promises that the natural flavor and purity of their potent gummies derived from hemp have been preserved through a CO2 extraction process and rigorous quality assurance analysis.

Lab tests that are publishable: these results have helped Delta Extrax gummies earn a good reputation. All test results are made accessible to the public on their webpage, demonstrating their commitment to transparency from the start of the process through the launch of the product. They also assist with consumer protection laws in the USA.

Cruelty-free: All of the components in such gummies are plant-based, and the aromas used were chosen with care to avoid animal cruelty. Because there are no artificial ingredients or preservatives, the food may be safely labeled as cruelty-free.

As a result of their pristine design and inherent safety, they are available for use by everyone. For your convenience, Delta Extrax Delta 9 gummies come in a variety of flavors and dosages throughout the day. "Daytime" and "Night-time" modes are available, with distinct features for each moment of the day.

Flavor: The comforting flavor of the Blueberry Bursts makes them a great choice for dessert after a hearty dinner. Nevertheless, they may try energizing drinks like Kiwi Mix as well as Guavaberry to keep them going strong all day.

Pros

  • Cannabidiol (also known as delta 9) gummy candies containing a synthetic variant of the active ingredient
  • Useful Educational Website
  • Unique Flavors, Delivered in a Number of Ways
  • Candy that is both sweet and chewy
  • Ensured return on investment
  • Components that are 100% pure and risk-free

Cons

  • Incentives for shipping are low, which is disappointing.

Customers’ Reviews

By practicing the comments, we realized that there were no problems. In all aspects, from the trustworthy packing to the delightful aftertaste, this item has indeed been warmly welcomed by its buyers.

The cognitive benefits of the legal, hemp-derived medicine Delta Extrax Delta 9 gummies have been documented by certain users.

Furthermore, they said that the pleasant flavor of Delta 9 THC added to its appeal because of its medicinal properties. They like candy, and they like how cheap they are.

=> Click here to visit the official website “Delta Extrax”

How We Made This List Of The Delta 9 Gummies

  • High Standards: Quality is usually at the top of the list when making a buying decision. Whether it's a car or a hat, everyone wants to know that it will perform as promised when they buy it. It may be difficult to evaluate a brand's quality, particularly one still finding its footing in the market. This evaluation, in addition to those from reputable labs, is what you should rely on most. Examine it carefully to ensure that it does not contain any potentially dangerous substances.
  • Significance of Hemp's Beginnings: For legal concerns, we made sure that only domestically grown hemp was utilized in our Delta 9 gummies. For instance, Exhale uses Colorado-grown hemp plants since it's a prime location for the plant. Several of the other delta 9 businesses we've looked at also import hemp components from places like Nevada and Kentucky.
  • Transparency: Please know that we never intend to put anyone in danger. We only recommend items that we feel do a great job of explaining to buyers what exactly is in them and how they should be used. Don't support businesses that use harmful chemicals or dubious additives in their products and then try to hide it. Companies that did not disclose their hemp origin or customer data were disqualified from further examination in order to maintain objectivity.
  • Independent Laboratory Testing: Third-party lab testing that was current and available to customers was required for all of the items we sold. Never put your money into hemp products before having a professional drug test performed on them. You should check the items to ensure they don't contain toxic substances or metals. The report should provide contact information for the laboratory in case the customer has any further questions. Every product we suggest is readily available for just such an assessment.
  • Opinions Voiced By Clients: Customer feedback may be quite illuminating. Online customer reviews are a great resource for finding information about a business. Since most of these firms haven't been operating well enough to have created a stable reputation, having heard from previous clients is an excellent approach to learning about how they conduct business. Before making a final decision, we read what consumers had to say about different items on a number of review sites.
  • Ways to Get What You Want: The sites' e-commerce capacities were also compared by our experts. We looked at how easy it was to do anything from window shopping to making a purchase to getting in touch with customer service to making a return.
  • Cancellations and exchanges: When making purchases on the web, we sought stores with reasonable return policies. Do not forget that you can always return an item if it does not fit or if it arrives damaged. We also needed to ensure that shipping costs and delivery time were reasonable. Some people use Delta-8 to relieve stress, depression, and physical discomfort. That's why we only stock products from companies that can get them to you quickly and cheaply.

Beginner’s Guide: Factors To Consider Before Buying Delta 9 THC Gummies

You should keep a few things in mind to get as much of your Delta 9 purchase. You can not make a good decision without first thinking about these things.

Check The Item's Safety

Because of the widespread presence of the toxin Delta 9, extreme care should be used before consuming any substance. First, check the label for ingredients' details and safety instructions in case of issues.

Next, pick a label whose quality can be Verified in a laboratory. Finally, pay close attention to the recommended dosage and note how the product affects you while taking it for the first time.

Competences of the Company

Before making a final decision, it's important to evaluate the delta 9 gummies' manufacturer. Furthermore, only a company with the proper expertise and resources can produce high-quality and the best delta 9 gummies .

Therefore, you shouldn't buy gummies from companies that boast the most about their products.

Instead, you should check the company's track record, the experience and credentials of its owners, and their dedication to innovation via research and development (R&D). What you learn might profoundly affect your opinion of the purchase.

The Trustworthiness of the Company

If a company is vague regarding the quality of its goods or services, you should select a different one.

Reviewing how other contented customers rate a product's reliability and durability might help you make a purchasing decision.

Also, consider the extent to which the brand's production standards are comparable to those of similar products.

Affordability

Saving cash is just one perk of buying delta 9 gummies digitally. Therefore, you should look for such delta 9 edibles companies that offer competitive pricing, prompt delivery, and flexible subscription plans.

Considering the high cost of production, any company offering shockingly low prices on THC gummies is likely to use cheap materials or questionable production techniques.

Find labels that are worth the price tag they set on themselves. If you locate a business with reasonable prices, you might consider joining their loyalty scheme to receive additional savings in return for your continued patronage.

The Product's Appeal and Flavor

Once you've established that a certain brand satisfies your first two requirements, you may go on to make your final selection. If you've never used this before, you should begin with the least effective dosage.

This may help you avoid overloading your system unintentionally. You want your product to have a satisfying flavor, so you are able to get the most out of using it.

Offering these sweets in a variety of tastes may sometimes increase their effect. Choose items keeping in mind when you'll be eating or drinking them.

The Seed from Which Hemp Grows

If a firm is forthright about its resources and methods, customers may feel more comfortable doing business with it.

Any retailer selling Delta 9 products without explaining where they obtain their hemp should be avoided.

This usually means it's of questionable quality or origins. Always choose items that include organically grown hemp from the United States.

FAQs: Delta 9 Gummies

Who Is It Designed to Serve?

It is recommended that only responsible adults use these high quality delta 9 gummies. However, they're great for anyone who would rather relax healthy and risk-free.

Effective in alleviating pain, tension, stress, and anxiety. Possible benefits include enhanced mental health and restful sleep.

How should I take these Delta 9 edibles?

If you want to get the result for the best Delta 9 gummies possible, do what it says on the label. Because of how little and easy to carry they are, you may enjoy one of these treats wherever you happen to be. Because of its psychotropic effects, however, responsible usage is essential.

The most conservative dosage for promoting inventiveness and concentration is 5 milligrams, taken every 4-8 hours.

Curious minds desire to know: Are there any negative side effects from taking these delta 9 gummies?

A few people who eat these sweets report experiencing adverse effects, including red eyes, dry mouth, dizziness, increased appetite, and drowsiness.

Just read the label if you want to know how much of the drug to take. Don't eat additional gummies if you would like them to kick in faster.

How Likely Are These Delta 9 Gummies to Interfere with My Medications?

You should see your primary care physician before using this product if you are presently on any form of medication. THC use may interfere with the metabolism of several medications.

Notifying your doctor that you're taking THC gummies might help you prevent any unwanted drug interactions. After that, bring the gummies in or pull up the website to present to your doctor before eating them.

When Will My Levels of Delta-9 THC Fall?

THC's half-life in the body after a single dose may vary greatly, but you can probably count on it being at a minimum of one month.

The reason is it may now be found in bodily fluids such as urine. The length of time it stays in your system is based on how often you use it and how many candies or milligrams you consume.

Is there any potential for damage if I consume these candies?

A possible side effect of eating Delta 9 Gummies is getting high. Nevertheless, the intensity of this high varies greatly from person to person.

Some individuals could find it simple, while others might find it difficult. If you want to prevent problems, always buy from reputable vendors.

If you've never used THC before, it's smart to ease into a tiny dose and monitor your reaction time before increasing the dosage. Because of the potential potency of delta 9 THC, appropriate dosing, especially when initially starting out, is essential. Be careful.

Can I purchase Delta 9 gummies digitally without the need for a prescription?

Delta-9, on the other hand, may be purchased online without a doctor's prescription. Delta 9 gummies may be legally purchased online with no prescription since they abide by the 2018 Hemp Farm Bill's criteria and have a delta 9 gummies content of slightly under 0.3percent depending on their dry weight.

On the open market, you may get delta 9 gummies with as much as 10 milligrams of THC. Increasing the gummy's potency without exceeding the THC weight limit would require making it unpleasantly large.

Therefore, delta 9 gummies, which may be purchased from federally legal available dispensaries, are a promising substitute for Delta-9 flowers for medical use since they do not need a physician's prescription.

These candies seem great, but is there any risk of dependency?

As these delta 9 gummies aren't really addictive, you may enjoy them without worrying about succumbing to constant cravings.

What Are The Most Potent Delta 9 Gummies?

As more people become aware of the calming effects of delta-9, cutting-edge new items have entered the market. Try some Delta 9 THC gummies made from hemp to experience the benefits of THC without drawing attention to yourself.

After a long and stressful day, nothing beats unwinding with one of these yummy delta 9 gummies. These sweets are available for purchase online and may be enjoyed at any time.

Use these sweets whenever you need a pick-me-up, whether you're at your residence or on the go. Before making a purchase, make sure the firm is legitimate by looking into its background, previous clients, and reviews.

Make sure they are using natural, high-quality substances that haven't been tampered with. Then, utilizing one of the best delta 9 gummy items mentioned in this post, we hope you should have a satisfying delta-9 encounter.

The above is a sponsored post, the views expressed are those of the sponsor/author and do not represent the stand and views of Outlook Editorial.

Tue, 07 Feb 2023 08:13:00 -0600 en text/html https://www.outlookindia.com/outlook-spotlight/best-delta-9-gummies-top-4-thc-edibles-of-2023-news-260151
Killexams : Hillcrest Hospital South Meets DNV Advanced Standards for Orthopedic Excellence

The MarketWatch News Department was not involved in the creation of this content.

Tulsa, OK, Feb 14, 2023 (GLOBE NEWSWIRE via COMTEX) -- Tulsa, OK, Feb. 14, 2023 (GLOBE NEWSWIRE) -- Hillcrest Hospital South has achieved designation as an Orthopedic Center of Excellence by DNV. They have the honor of being the first hospital in Oklahoma to reach this prestigious milestone.

"Certification of orthopedic programs is a valuable tool for measuring program excellence. We congratulate Hillcrest on their achievement and are honored to have them as a part of the DNV family," stated Ronell Myburgh MHA, MBA, BSN, RN, Director, Certifications for DNV Healthcare USA Inc.

Achieving Orthopedic Center of Excellence designation requires that a hospital obtain advanced certification with DNV in at least three (3) of their orthopedic service line programs. Hillcrest Hospital South has achieved advanced certification of their Hip & Knee Replacement, Spine Surgery, and Shoulder Surgery Programs. The certification requirements are based on industry standards and evidence-based practices. The process for becoming certified includes a rigorous onsite survey by DNV. These Advanced Orthopedic Certifications are recognized by both the Blue Cross Blue Shield Blue Distinction Program and the Aetna Institutes of Quality (IOQ) Program.

Bennett Geister, CEO of Hillcrest Hospital South, stated, "Over the past five years, Orthopedic surgery has been one of the highest growth service lines at Hillcrest South. We needed to ensure that our safety and quality outcomes continued to elevate with our volumes, and hence, we pursued center of excellence designation to put our program in line with the best programs in the country." Geister further stated, "Our team came together to implement and adopt best practices so that the patient's experience is top of class when they trust their care to Hillcrest Hospital South. This is a great achievement driven by our staff doing the work, and I'm excited to showcase our program to the communities we serve."

"Our innovative hospital accreditation and certification programs create trust between communities and their hospitals," stated David Tellez, Regional Lead, DNV Supply Chain and Product Assurance, "Patients can feel confident in their care knowing the hospital has met our rigorous standards for safety and quality."

About Hillcrest Healthcare System

Hillcrest South, a 180-bed hospital, is an acute care medical center located in south Tulsa. Hillcrest South offers a wide range of inpatient and outpatient services including maternity, cardiology, emergency, wound care, orthopedics, and surgery. To learn more, visit hillcrestsouth.com.

About DNV

DNV is a global independent certification, assurance and risk management provider, operating in more than 100 countries. Through its broad experience and deep expertise, DNV advances safety and sustainable performance, sets industry benchmarks, drives innovative solutions.

Whether certifying a company's management system or products, accrediting hospitals, providing training, assessing supply chains or digital assets, DNV enables customers and stakeholders to make critical decisions with confidence, continually Boost and realize long-term strategic goals sustainably.

DNV draws on its wide technical and industry expertise to help companies worldwide build consumer and stakeholder trust. Driven by its purpose, to safeguard life, property, and the environment, DNV helps tackle the challenges and global transformations facing its customers and the world today and is a trusted voice for many of the world's most successful and forward-thinking companies.

For more information about DNV, visit www.dnvhealthcare.com.

Attachment

Randi Hamilton
DNV Healthcare USA Inc.
513-313-0790
randi.hamilton@dnv.com

COMTEX_424460123/2471/2023-02-14T06:00:50

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(C) Copyright 2023 GlobeNewswire, Inc. All rights reserved.

The MarketWatch News Department was not involved in the creation of this content.

Mon, 13 Feb 2023 20:00:00 -0600 en-US text/html https://www.marketwatch.com/press-release/hillcrest-hospital-south-meets-dnv-advanced-standards-for-orthopedic-excellence-2023-02-14
Killexams : Jazz Chisholm Jr.’s development in center field will play key role in Marlins’ 2023 success

One of the biggest decisions surrounding the Miami Marlins’ offseason — and one of the biggest decisions that could determine their success in 2023 — didn’t necessarily involve the transaction log.

It came in early January, before the Marlins had made any of the handful of moves that transformed their roster ahead of spring training. After a get-together, rising star Jazz Chisholm Jr. pulled first-year manager Skip Schumaker aside to pass along a clear message.

“I’m wiling to do whatever you want,” Schumaker recalled Chisholm telling him. “If you need me in center field, if you need me at shortstop, if you need me at second, whatever you need, I’m willing to help you win and help our team win.”

A couple weeks later, after the Marlins signed infielder Jean Segura and traded for infielder Luis Arraez, the decision became official: Chisholm, the Marlins’ starting second baseman the past two seasons and a 2022 All-Star at that spot, would be moving to center field.

Now, both Chisholm and Schumaker know the move most likely won’t be a seamless transition. Chisholm has never played in the outfield before and there are a lot of intricacies with learning the position — tracking balls, positioning, learning the warning tracks, adjusting to the dimensions of the ballpark, cutoff throws, the list goes on.

But if Chisholm can learn to handle the position with his speed and raw athleticism, it will solve one of the Marlins’ longstanding problems over the past few seasons.

“When you’re a rookie manager and you have your best player say that to you, that’s a big deal,” Schumaker said. “It’s kind of like you can take a deep breath and you’re like ‘OK. This guy’s in it to win.’ You don’t know the guys you’re acquiring as a manager and when your best player — the face of MLB The Show — is willing to do anything, that’s a big deal.”

Added Marlins general manager Kim Ng: “I think Jazz is a very unique athlete,” Ng said. “He’s very dynamic. He’s got great range, great speed. A lot of things that you look for when you’re thinking about center field. We’ve seen him grow. We’ve seen how he handles pop ups and ranges to the ones that are tough to get to.”

Chisholm has been taking regular reps in center field for the past month now, ever since he had the meeting with Schumaker. He has worked extensively with new Marlins first base coach and outfield coach Jon Jay and said he has arranged a meeting with 13-time All-Star Ken Griffey Jr. to get tips on playing center field. Chisholm also has a long history with Marlins alumnus Juan Pierre, who started 1,143 career games in center.

“It’s going great so far,” Chisholm said. “Not many dropped balls. I dropped a couple of bare hand balls but with the glove on, I’m feeling pretty good that I’ll catch everything.”

Chisholm said having grown up as a middle infielder will help ease the transition to the outfield in terms of reaction time to plays.

“It’s just gonna be fun out there,” Chisholm said.

And, he also hopes, it will help the Marlins turn the corner after a 69-93 season.

With Chisholm in center field, it freed the Marlins up to acquire a pair of contact-oriented batters in Segura and Arraez without there being a logjam in the infield. Arraez is primarily going to play second base and back up Garrett Cooper at first base. Segura is slated to play third base with Joey Wendle rounding out the group at shortstop.

“I feel like this year the clubhouse really has that winning attitude,” Chisholm said. “The positivity that everybody walks in with, with their chest and their head held high. I’m talking to guys and everybody can’t wait to get on the field. They can’t wait to play. They can’t wait to do this. It wasn’t like that before. ... Now, it’s time to win. That’s what we are about right now.”

Other story lines to follow

Who closes?: Righties Dylan Floro and Matt Barnes as well as lefty Tanner Scott all appear to factor into the equation. Each logged at least 20 saves over the past two seasons, giving Miami the option to mix and match in the ninth inning based on matchups unless one of the three takes command of the role.

Rule changes: Pitch clocks, no shifts, fewer pickoff attempts and larger bases are all coming to the game this season. Teams will use spring training to adjust to the new rules and find ways to use them to their benefits.

The World Baseball Classic: The international tournament takes place from March 8-21. Five players on the Marlins’ 40-man roster — including three members of the projected starting rotation (Sandy Alcantara, Johnny Cueto and Jesus Luzardo) and two top-of-the-lineup hitters (Arraez and Segura) — are slated to participate, meaning they will miss a majority of the back half of spring training.

Top prospects: Thirteen of the Marlins’ top-30 prospects according to MLB Pipeline will participate in big-league camp this season. The group is headlined by Eury Perez, the 19-year-old right-handed pitcher who is a near consensus top-10 prospect in all of baseball. 2022 first-round pick infielder Jacob Berry and 2020 second-round pick left-handed pitcher Dax Fulton also highlight the prospects attending camp.

Max Meyer, Miami’s second-ranked prospect, is not included in this group of 13 as he continues to rehab from Tommy John surgery.

Sixto Sanchez: The former phenom right-handed pitcher made pitcher made his MLB debut in 2020 to great fanfare. He hasn’t been seen in a regular-season game since after dealing with an assortment of shoulder issues that have resulted in two separate surgeries.

Sanchez is heading into camp lighter — he said he has lost 46 pounds — and has already thrown five bullpens ahead of reporting to Jupiter. He hasn’t been cleared for Grapefruit League games just yet but feels he is trending in the direction of being able to play.

“It was very, very hard for me the last couple of years,” Sanchez said Friday. “You watch the games, you see your teammates playing and you really want to be there. The frustration was really high and it wasn’t easy for me to maintain a positive attitude. It was really hard because it was just setback after setback and just trying to come back and trying to maintain that positive energy. It was very difficult, but thank goodness we’re where we are right now and looking forward.”

New coaching staff’s impact: Schumaker retained just three coaches from last year’s staff — pitching coach Mel Stottlemyre Jr., bullpen coach Wellington Cepeda and bullpen coordinator Rob Flippo. He promoted Jody Reed from minor-league infield coordinator to third-base coach and infield coach on the MLB staff.

Everyone else is new. In addition to Jay, the coaching staff includes bullpen coach Luis Urueta, hitting coach Brant Brown, assistant hitting coaches John Mabry and Jason Hart, quality assurance coach Griffin Benedict and field coordinator Rod Barajas.

Cooper called Brown “as eager of a hitting coach and as ready to go as I’ve seen in my time here.”

“He texts me every other day, it seems like,” Cooper said. “It’s a very hands-on approach that we haven’t had for the past few years where we’re breaking down video after almost every swing.”

Sat, 11 Feb 2023 00:45:00 -0600 en-US text/html https://www.aol.com/news/jazz-chisholm-jr-development-center-154510164.html
Killexams : Final Weeks To Register For The 2 Day Introduction To Computer System Validation Online Course (March 27-28, 2023)
(MENAFN- GlobeNewsWire - Nasdaq)

Dublin, Feb. 06, 2023 (GLOBE NEWSWIRE) -- The 'introduction to computer system validation' training has been added to ResearchAndMarkets.com's offering.

Computer system validation has been regulated by FDA for more than 30 years, as it relates to systems used in the manufacturing, testing and distribution of a product in the pharmaceutical, biotechnology, medical device or other FDA-regulated industries. The FDA requirements ensure thorough planning, implementation, integration, testing and management of computer systems used to collect, analyze and/or report data.

Electronic records and electronic signatures (ER/ES) came into play through guidelines established by FDA in 1997, and disseminated through 21 CFR Part 11.This code describes the basic requirements for validating and documenting ER/ES capability in systems used in an FDA-regulated environment.

In the early 2000s, FDA recognized they could not inspect every computer system at every regulated company and placed the onus on industry to begin assessing all regulated computer systems based on risk. The level of potential risk, should the system fail to operate properly, needed to be the basis for each company's approach to developing a validation approach and rationale as part of the planning process. System size, complexity, business criticality, GAMP 5 category and risk rating are the five key components for determining the scope and robustness of testing required to ensure data integrity and product safety.

We will explore the best practices and strategic approach for evaluating computer systems used in the conduct FDA-regulated activities and determining the level of potential risk, should they fail, on data integrity, process and product quality, and consumer/patient safety. We will walk through the System Development Life Cycle (SDLC) approach to validation, based on risk assessment, and will also discuss 21 CFR Part 11 and the importance of managing electronic records and signatures appropriately.

We'll talk about CSA and how to validate cloud, COTS, SaaS, and other systems and maintain them in a validated state. This will include a discussion around waterfall, agile, and other methodologies for system development, testing, and validation, including how to apply automated testing to your approach.

We will also walk through the entire set of essential policies and procedures, as well as other supporting documentation and activities that must be developed and followed to ensure compliance. We will provide an overview of practices to prepare for an FDA inspection, and will also touch on the importance of auditing vendors of computer system hardware, software, tools and utilities, and services.

Finally, we will provide an overview of industry best practices, with a focus on data integrity and risk assessment that can be leveraged to assist in all your GxP work.

CSV Training Overview

FDA's exact focus on data integrity during computer system validation inspections and audits has brought this issue to the forefront of importance for compliance of systems used in regulated industries. These include all systems that 'touch' product, meaning they are used to create, collect, analyze, manage, transfer and report data regulated by FDA.

All structured data, including databases, and unstructured data, including documents, spreadsheets, presentations, images, audio and video files, amongst others, must be managed and maintained with integrity throughout their entire life cycle.It is a risk-based approach to Computer System Validation (CSV) and maintenance of a system in a validated state that leads to the best results and compliance with FDA's expectations.

Why Should You Attend

This seminar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle (SDLC) Methodology when validating computer systems subject to FDA regulations. This is critical in order to develop the appropriate validation strategy and achieve the thoroughness required to prove that a system does what it purports to do, and a key element is a thorough risk assessment.

It also ensures that a system is maintained in a validated state throughout its entire life cycle, from conception through retirement, making it critical to continue assessing risk as changes are made. We will discuss the phases within the SDLC, and how these form the basis for any CSV project. The importance of the sequence of steps will also be covered.

We will also cover the exact draft guidance from FDA on Computer Software Assurance (CSA), which is based on critical thinking in approach. We'll talk about agile vs. waterfall, automated testing, Cloud, COTS, and Software-as-a-Service. We'll also touch on 21 CFR Part 11, FDA's guidance on electronic records/signatures to discuss the importance of including aspects of er/es technology during validation and maintenance of a system.

Learning Objectives

    Learn how to identify 'GxP' Systems Discuss the Computer System Validation (CSV) approach based on FDA requirements Learn about the System Development Life Cycle (SDLC) approach to validation Learn about COTS, cloud, SaaS and other types of systems and how they can be validated and maintained in a validated state. Understand FDA's new draft guidance on Computer Software Assurance (CSA) and how to apply this to your approach to validation, focusing on critical thinking. Discuss the best practices for documenting computer system validation efforts, including requirements, design, development, testing and operational maintenance procedures Understand how to maintain a system in a validated state through the system's entire life cycle Learn how to assure the integrity of data that supports GxP work Discuss the importance of 'GxP' documentation that complies with FDA requirements Learn about the policies and procedures needed to support your validation process and ongoing maintenance of your systems in a validated state Understand the key components of 21 CFR Part 11 compliance for electronic records and signatures Know the regulatory influences that lead to FDA's current thinking at any given time Learn how to conduct a risk assessment on computer systems that will provide the basis for developing a validation rationale Understand the need to include an assessment of a computer system's size, complexity, business criticality, GAMP 5 category and risk, should it fail, to develop a cohesive and comprehensive validation rationale Learn how to assess risk, based on probability of occurrence, severity of impact, detectability and mitigation, along with technical and procedural controls that can help minimize risk Learn how to best prepare for an FDA inspection or audit of a GxP computer system Understand the importance of performing a thorough vendor audit to ensure oversight to the products and services they deliver Finally, understand the industry best practices that will enable you to optimize your approach to validation and compliance, based on risk assessment, to ensure data integrity is maintained throughout the entire data life cycle Q&A

Who Should Attend:

    Information Technology Analysts Information Technology Managers QC/QA Managers QC/QA Analysts Clinical Data Managers Clinical Data Scientists Analytical Chemists Compliance Managers Laboratory Managers Automation Analysts Manufacturing Managers Manufacturing Supervisors Supply Chain specialists Computer System Validation specialists GMP Training specialists Business Stakeholders responsible for computer system validation planning, execution, reporting, compliance, maintenance and audit Consultants working in the life sciences industry who are involved in computer system implementation, validation and compliance Auditors engaged in internal inspection

For more information about this training visit

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Sun, 05 Feb 2023 21:10:00 -0600 Date text/html https://menafn.com/1105529386/Final-Weeks-To-Register-For-The-2-Day-Introduction-To-Computer-System-Validation-Online-Course-March-27-28-2023
Killexams : One Month Until the Introduction to Computer System Validation Course (April 17-18, 2023)

Company Logo

Dublin, Feb. 06, 2023 (GLOBE NEWSWIRE) -- The "Introduction to Computer System Validation" training has been added to ResearchAndMarkets.com's offering.

Computer system validation has been regulated by FDA for more than 30 years, as it relates to systems used in the manufacturing, testing and distribution of a product in the pharmaceutical, biotechnology, medical device or other FDA-regulated industries.The FDA requirements ensure thorough planning, implementation, integration, testing and management of computer systems used to collect, analyze and/or report data.

Electronic records and electronic signatures (ER/ES) came into play through guidelines established by FDA in 1997, and disseminated through 21 CFR Part 11.This code describes the basic requirements for validating and documenting ER/ES capability insystems used in an FDA-regulated environment.

In the early 2000s, FDA recognized they could not inspect every computer system at every regulated company and placed the onus on industry to begin assessing all regulated computer systems based on risk.The level of potential risk, should the system fail to operate properly, needed to be the basis for each company's approach to developing a validation approach and rationale as part of the planning process.System size, complexity, business criticality, GAMP 5 category and risk rating are the five key components for determining the scope and robustness of testing required to ensure data integrity and product safety.

We will explore the best practices and strategic approach for evaluating computer systems used in the conduct FDA-regulated activities and determining the level of potential risk, should they fail, on data integrity, process and product quality, and consumer/patient safety.We will walk through the System Development Life Cycle (SDLC) approach to validation, based on risk assessment, and will also discuss 21 CFR Part 11 and the importance of managing electronic records and signatures appropriately.

We'll talk about CSA and how to validate cloud, COTS, SaaS, and other systems and maintain them in a validated state. This will include a discussion around waterfall, agile, and other methodologies for system development, testing, and validation, including how to apply automated testing to your approach.

We will also walk through the entire set of essential policies and procedures, as well as other supporting documentation and activities that must be developed and followed to ensure compliance.We will provide an overview of practices to prepare for an FDA inspection, and will also touch on the importance of auditing vendors of computer system hardware, software, tools and utilities, and services.

Finally, we will provide an overview of industry best practices, with a focus on data integrity and risk assessment that can be leveraged to assist in all your GxP work.

CSV Training Overview

FDA's exact focus on data integrity during computer system validation inspections and audits has brought this issue to the forefront of importance for compliance of systems used in regulated industries.These include all systems that "touch" product, meaning they are used to create, collect, analyze, manage, transfer and report data regulated by FDA.All structured data, including databases, and unstructured data, including documents, spreadsheets, presentations, images, audio and video files, amongst others, must be managed and maintained with integrity throughout their entire life cycle.It is a risk-based approach to Computer System Validation (CSV) and maintenance of a system in a validated state that leads to the best results and compliance with FDA's expectations.

Learning Objectives

  • Learn how to identify "GxP" Systems

  • Discuss the Computer System Validation (CSV) approach based on FDA requirements

  • Learn about the System Development Life Cycle (SDLC) approach to validation

  • Learn about COTS, cloud, SaaS and other types of systems and how they can be validated and maintained in a validated state.

  • Understand FDA's new draft guidance on Computer Software Assurance (CSA) and how to apply this to your approach to validation, focusing on critical thinking.

  • Discuss the best practices for documenting computer system validation efforts, including requirements, design, development, testing and operational maintenance procedures

  • Understand how to maintain a system in a validated state through the system's entire life cycle

  • Learn how to assure the integrity of data that supports GxP work

  • Discuss the importance of "GxP" documentation that complies with FDA requirements

  • Learn about the policies and procedures needed to support your validation process and ongoing maintenance of your systems in a validated state

  • Understand the key components of 21 CFR Part 11 compliance for electronic records and signatures

  • Know the regulatory influences that lead to FDA's current thinking at any given time

  • Learn how to conduct a risk assessment on computer systems that will provide the basis for developing a validation rationale

  • Understand the need to include an assessment of a computer system's size, complexity, business criticality, GAMP 5 category and risk, should it fail, to develop a cohesive and comprehensive validation rationale

  • Learn how to assess risk, based on probability of occurrence, severity of impact, detectability and mitigation, along with technical and procedural controls that can help minimize risk

  • Learn how to best prepare for an FDA inspection or audit of a GxP computer system

  • Understand the importance of performing a thorough vendor audit to ensure oversight to the products and services they deliver

  • Finally, understand the industry best practices that will enable you to optimize your approach to validation and compliance, based on risk assessment, to ensure data integrity is maintained throughout the entire data life cycle

  • Q&A

Agenda

DAY 1

01:00pm - 02:00pm:

Module 1:CSV Methods and Models

  • GxP Systems

  • Computer System Validation (CSV)

  • Common SDLC Methodologies

  • GAMP5 "V" Model

  • Computer System Validation (CSV) vs. Computer Software Assurance (CSA)

  • Critical Thinking

  • Waterfall vs. Agile Methodology

Module 2:Software and Services

  • Computer Off-the-Shelf (COTS) Software

  • FDA's "Case for Quality"

  • Cloud Systems

  • Software as a Service (SaaS)

  • Platform as a Service (PaaS) & Infrastructure as a Service (IaaS)

  • Single Sign On (SSO)

  • Medical Devices and Software as a Medical Device (SaaMD)

  • Mobile Devices and Medical Application

  • Spreadsheet Validation

2:00pm-2:10pm - 10 min Break

2:10pm-3:50pm:

Module 3: CSV Planning

  • Validation Strategy Document (VSD)

  • Validation Strategy Components

  • Rationale for Validation Testing

  • GAMP5 System Categorization

  • Risk Assessment

  • Risk Mitigation

  • Exercise: Risk Assessment

Module 4:System Requirements and Design

  • Requirements Development

  • User Requirements Specification (URS)

  • Functional Requirements Specification (FRS)

  • System Design/Configuration Management Specification (SDS/CMS)

  • Exercise: Application and Design

3:50pm-4:00pm - Q&A

DAY 2

1:00pm-2:30pm

Module 5:IQ, OQ, PQ Test Planning&Execution

Module 6:Test and Validation Reports

  • Requirements Traceability Matrix (RTM) Purpose and Contents

  • Validation Summary Report (VSR) Purpose and Contents

  • System Acceptance and Release Notification

Module 7: CSV Operations and Maintenance

  • Maintaining a System in a Validated State

  • Disaster Recovery Planning

  • Business Continuity Planning

  • Record Retention

  • System Retirement Challenges

  • Legacy Systems and Integration

  • Data Migration

Module 8:CSV Supporting Components

  • Good Documentation Practices (GDPs)

  • Training

  • Organizational Change Management (OCM)

  • CSV Policies and Procedures

2:30pm-3:50pm:

Module 9:Managing FDA-Regulated Data

Module 10: Vendor Audit

  • Audit Preparation

  • Audit Execution

  • Post-Audit

4:15pm-4:50pm:

Module 11:FDA Trends

Module 12:Inspection Preparation

  • FDA Inspection Readiness

  • Industry Best Practices

4:50pm-5:00pm - Q&A

Additional material that can be read through and completed off-line after the presentation is completed:

  • CSV Exercises (These can be done after the session)

  • Exercise 1:CSV

  • Exercise 2:Validation Master Plan (VMP) Writing

  • Exercise 3:FDA Requirements for ER/ES

  • Exercise 4:Interviews and URS/FRS Writing

  • Exercise 5:IQ, OQ, PQ Test Protocol Writing

  • Exercise 6:RTM Writing

  • Exercise 7:Be the Consultant


Speakers:

Carolyn Troiano
Webinar/Seminar/Workshop Instructor in FDA Compliance Training

Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs

For more information about this training visit https://www.researchandmarkets.com/r/mg19w2

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