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  2. Pharmaceutical Inspection Convention and Pharmaceutical ...

    en.wikipedia.org/wiki/Pharmaceutical_Inspection...

    The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S) are two international instruments between countries and pharmaceutical inspection authorities. The PIC/S is meant as an instrument to improve co-operation in the field of Good Manufacturing Practices between regulatory authorities and the ...

  3. Global Monitoring Plan - Wikipedia

    en.wikipedia.org/wiki/Global_Monitoring_Plan

    The Global Monitoring Plan (GMP) under the Stockholm Convention on Persistent Organic Pollutants is a programme that enables collection of comparable monitoring data from all regions of the world to assess the effectiveness of the Stockholm Convention in minimizing human and environmental exposure to persistent organic pollutants (POPs).

  4. Good manufacturing practice - Wikipedia

    en.wikipedia.org/wiki/Good_manufacturing_practice

    Current good manufacturing practices (cGMP) are those conforming to the guidelines recommended by relevant agencies. Those agencies control the authorization and licensing of the manufacture and sale of food and beverages , [ 1 ] cosmetics , [ 2 ] pharmaceutical products , [ 3 ] dietary supplements , [ 4 ] and medical devices . [ 5 ]

  5. Pharmaceutical industry - Wikipedia

    en.wikipedia.org/wiki/Pharmaceutical_industry

    A drug manufacturer inspection by the US Food and Drug Administration. The pharmaceutical industry is a medical industry that discovers, develops, produces and markets pharmaceutical goods for use as drugs that are then administered to (or self-administered by) patients.

  6. 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 ...

  7. 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.

  8. Cyclic guanosine monophosphate - Wikipedia

    en.wikipedia.org/wiki/Cyclic_guanosine_monophosphate

    Cyclic guanosine monophosphate (cGMP) is a cyclic nucleotide derived from guanosine triphosphate (GTP). cGMP acts as a second messenger much like cyclic AMP.Its most likely mechanism of action is activation of intracellular protein kinases in response to the binding of membrane-impermeable peptide hormones to the external cell surface. [1]

  9. GMP - Wikipedia

    en.wikipedia.org/wiki/GMP

    GmP, a category of mixed train in German-speaking countries; Gimpo International Airport (IATA code), Seoul, South Korea; Martin GMP, an American transport aircraft; Gaobeidian East railway station (telegraph code), China Railway; Hyundai Electric Global Modular Platform, a platform for electric cars