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  2. Verification and validation - Wikipedia

    en.wikipedia.org/wiki/Verification_and_validation

    Verification is intended to check that a product, service, or system meets a set of design specifications. [6] [7] In the development phase, verification procedures involve performing special tests to model or simulate a portion, or the entirety, of a product, service, or system, then performing a review or analysis of the modeling results.

  3. Validation and verification (medical devices) - Wikipedia

    en.wikipedia.org/wiki/Validation_and...

    To establish a reference range, the Clinical and Laboratory Standards Institute (CLSI) recommends testing at least 120 patient samples. In contrast, for the verification of a reference range, it is recommended to use a total of 40 samples, 20 from healthy men and 20 from healthy women, and the results should be compared to the published reference range.

  4. Software verification and validation - Wikipedia

    en.wikipedia.org/wiki/Software_verification_and...

    Software verification and validation. In software project management, software testing, and software engineering, verification and validation is the process of checking that a software engineer system meets specifications and requirements so that it fulfills its intended purpose. It may also be referred to as software quality control.

  5. RightspotpH Indicator - Wikipedia

    en.wikipedia.org/wiki/RightspotpH_Indicator

    The effectiveness of the RightSpotpH® Indicator has been validated through clinical studies. A significant study published in the International Journal of Emergency Medicine demonstrated that the device is sensitive and specific for determining intragastric pH levels below or above 4.5, a common threshold used for confirming nasogastric tube placement.

  6. Good laboratory practice - Wikipedia

    en.wikipedia.org/wiki/Good_Laboratory_Practice

    The Principles of Good Laboratory Practice (GLP) establish rules and criteria for a quality system that oversees the organizational processes and conditions in which non-clinical health and environmental safety studies are planned, conducted, monitored, recorded, reported, and archived.

  7. Validation (drug manufacture) - Wikipedia

    en.wikipedia.org/wiki/Validation_(drug_manufacture)

    Validation (drug manufacture) The process of establishing documentary evidence demonstrating that a procedure, process, or activity carried out in testing and then production maintains the desired level of compliance at all stages. In the pharmaceutical industry, it is very important that in addition to final testing and compliance of products ...

  8. Engineering validation test - Wikipedia

    en.wikipedia.org/wiki/Engineering_validation_test

    Engineering validation test. An engineering verification test (EVT) is performed on first engineering prototypes, to ensure that the basic unit performs to design goals and specifications. [1] Verification ensures that designs meets requirements and specification while validation ensures that created entity meets the user needs and objectives.

  9. Software assurance - Wikipedia

    en.wikipedia.org/wiki/Software_Assurance

    Software assurance (SwA) is a critical process in software development that ensures the reliability, safety, and security of software products. [1] It involves a variety of activities, including requirements analysis, design reviews, code inspections, testing, and formal verification. One crucial component of software assurance is secure coding ...