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  2. 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).

  3. 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]

  4. EudraGMP - Wikipedia

    en.wikipedia.org/wiki/EudraGMP

    The database serves as a quick reference for checking the good manufacturing practice (GMP) of a potential contract manufacturer. One can search by the “company name, location, or certificate number and find details on the types of products or activities that the company conducts and the date of the most recent GMP inspection.” [3]

  5. Certificate of analysis - Wikipedia

    en.wikipedia.org/wiki/Certificate_of_analysis

    A certificate of analysis can be associated with cannabis and cannabis-derived products, attesting to their laboratory analysis for cannabinoids, adulterants, heavy metals, pesticides, mold, etc. This gives consumers "an easy way to review test results from responsible companies selling cannabis and cannabis-infused products".

  6. Product certification - Wikipedia

    en.wikipedia.org/wiki/Product_certification

    product certifications (many nations) Product certification or product qualification is the process of certifying that a certain product has passed performance tests and quality assurance tests, and meets qualification criteria stipulated in contracts, regulations, or specifications (sometimes called "certification schemes" in the product certification industry).

  7. European Directorate for the Quality of Medicines & HealthCare

    en.wikipedia.org/wiki/European_Directorate_for...

    Granted after an assessment of the documentation submitted by the applicant, a Certificate of Suitability (CEP) [18] provides proof that the methods used by a manufacturer or distributor result in an product whose quality complies with the requirements laid down in the corresponding Ph. Eur. monograph(s). The EDQM also runs an inspection ...

  8. Nets reportedly trading Dennis Schröder to Warriors for De ...

    www.aol.com/nets-reportedly-trading-dennis...

    Schröder has averaged 18.4 points and 6.6 assists per game this season, his first full one with the Nets. They traded for him midway through last season with the Toronto Raptors.

  9. 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 ...

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