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  2. Monitoring and evaluation - Wikipedia

    en.wikipedia.org/wiki/Monitoring_and_evaluation

    Monitoring and evaluation. Monitoring and Evaluation ( M&E) is a combined term for the processes set up by organizations such as companies, government agencies, international organisations and NGOs, with the goal of improving their management of outputs, outcomes and impact. Monitoring includes the continuous assessment of programmes based on ...

  3. Certificate Transparency - Wikipedia

    en.wikipedia.org/wiki/Certificate_Transparency

    Certificate Transparency. Certificate Transparency ( CT) is an Internet security standard for monitoring and auditing the issuance of digital certificates. [1] When an internet user interacts with a website, a trusted third party is needed to assure the user that the website is legitimate and that the website's encryption key is valid.

  4. Monitoring in clinical trials - Wikipedia

    en.wikipedia.org/wiki/Monitoring_in_clinical_trials

    Clinical monitoring is the oversight and administrative efforts that monitor a participant's health and efficacy of the treatment during a clinical trial.Both independent and government-run grant-funding agencies, such as the National Institutes of Health (NIH) and the World Health Organization (WHO), require data and safety monitoring protocols for Phase I and II clinical trials conforming to ...

  5. List of abbreviations used in medical prescriptions - Wikipedia

    en.wikipedia.org/wiki/List_of_abbreviations_used...

    This is a list of abbreviations used in medical prescriptions, including hospital orders (the patient-directed part of which is referred to as sig codes).This list does not include abbreviations for pharmaceuticals or drug name suffixes such as CD, CR, ER, XT (See Time release technology § List of abbreviations for those).

  6. History of the Food and Drug Administration - Wikipedia

    en.wikipedia.org/wiki/History_of_the_Food_and...

    FDA history. Origins of federal food and drug regulation. The 1906 Pure Food and Drug Act and creation of the FDA. The 1938 Food, Drug, and Cosmetic Act. Regulation of human drugs and medical devices after 1938. Early FD&C Act amendments: 1938–1958. Expansion of premarket approval process: 1959–1985. FDA reforms in the AIDS era.

  7. Mandatory reporting in the United States - Wikipedia

    en.wikipedia.org/wiki/Mandatory_reporting_in_the...

    Film Developers (for child pornography purposes) As of April 2019, any person who suspects child abuse or neglect is required to report suspected abuse or neglect regardless of profession in 18 States and Puerto Rico. In all other States, territories, and the District of Columbia, any person is permitted to report.

  8. Verification and validation - Wikipedia

    en.wikipedia.org/wiki/Verification_and_validation

    Overview Verification. Verification is intended to check that a product, service, or system meets a set of design specifications. 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.

  9. Medical test - Wikipedia

    en.wikipedia.org/wiki/Medical_test

    A medical test is a medical procedure performed to detect, diagnose, or monitor diseases, disease processes, susceptibility, or to determine a course of treatment. Medical tests such as, physical and visual exams, diagnostic imaging, genetic testing, chemical and cellular analysis, relating to clinical chemistry and molecular diagnostics, are typically performed in a medical setting.