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  2. Good manufacturing practice - Wikipedia

    en.wikipedia.org/wiki/Good_manufacturing_practice

    Operators must be trained to carry out and document procedures. Records must be made, manually or electronically, during manufacture that demonstrate that all the steps required by the defined procedures and instructions were in fact taken and that the quantity and quality of the food or drug was as expected.

  3. Contract manufacturing organization - Wikipedia

    en.wikipedia.org/wiki/Contract_manufacturing...

    A contract manufacturing organization (CMO), more recently referred to (and more commonly used now) as a contract development and manufacturing organization (CDMO) to avoid the acronym confusion of Chief Medical Officer or Clinical Monitoring Organization in the pharma industry, is a company that serves other companies in the pharmaceutical industry on a contract basis to provide comprehensive ...

  4. Good automated manufacturing practice - Wikipedia

    en.wikipedia.org/wiki/Good_Automated...

    GAMP itself was founded in 1991 in the United Kingdom to deal with the evolving U.S. Food and Drug Administration expectations for good manufacturing practice (GMP) compliance of manufacturing and related systems. [4] GAMP published its first guidance in 1994.

  5. Good engineering practice - Wikipedia

    en.wikipedia.org/wiki/Good_Engineering_Practice

    Good manufacturing practice (GMP) Best practice; American National Standards Institute (ANSI) Institute of Electrical and Electronics Engineers (IEEE) European Medicines Agency (EMEA) Food and Drug Administration (FDA) Ministry of Health, Labour and Welfare (Japan) Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation ...

  6. GxP - Wikipedia

    en.wikipedia.org/wiki/GxP

    GxP is a general abbreviation for the "good practice" quality guidelines and regulations. The "x" stands for the various fields, including the pharmaceutical and food industries, for example good agricultural practice, or GAP.

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  8. Certificate of pharmaceutical product - Wikipedia

    en.wikipedia.org/wiki/Certificate_of...

    The certificate of pharmaceutical product (abbreviated: CPP) is a certificate issued in the format recommended by the World Health Organization (WHO), which establishes the status of the pharmaceutical product and of the applicant for this certificate in the exporting country; [1] it is often mentioned in conjunction with the electronic Common Technical Document (eCTD).

  9. Occupational licensing - Wikipedia

    en.wikipedia.org/wiki/Occupational_licensing

    License portability refers to the legal concept where states (or other subnational certifying jurisdictions) recognize other jurisdictions licenses. Some states have mutual recognition with other states' certification either by their own state law or through interstate compact , however there are limited national standards in the United States ...