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  2. Good documentation practice - Wikipedia

    en.wikipedia.org/wiki/Good_documentation_practice

    Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.

  3. Distributed practice - Wikipedia

    en.wikipedia.org/wiki/Distributed_Practice

    Distributed practice is the most efficient method of procedural learning [citation needed]. By equally distributing the amount of practice of a given activity over a period of time, you will increase the efficiency of learning that skill.

  4. Pharmaceutical distribution - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_distribution

    In the US, Good Manufacturing Practice (GMP) Regulations are based on the Code of Federal Regulations 21 CFR 210/211, and USP 1079. The US Drug Supply and Chain Security Act (DSCSA), was enacted by Congress on November 26, 2013 and outlines requirements to build electronic systems that identify and trace prescription drugs distributed in the US ...

  5. 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.

  6. Best practice - Wikipedia

    en.wikipedia.org/wiki/Best_practice

    Good operating practice is a strategic management term. More specific uses of the term include good agricultural practices, good manufacturing practice, good laboratory practice, good clinical practice, and good distribution practice.

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  8. Regulation of therapeutic goods - Wikipedia

    en.wikipedia.org/.../Regulation_of_therapeutic_goods

    Drugs are classified under five headings. Under retail and distribution: [citation needed] Schedule X drugs - narcotics; Schedule H and L - injectables, antibiotics, antibacterials; Schedule C and C1 - biological products, for example serums and vaccines; Under manufacturing practice:

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