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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. Medicines and Healthcare products Regulatory Agency

    en.wikipedia.org/wiki/Medicines_and_Healthcare...

    The MHRA has several independent advisory committees which provide the UK Government with information and guidance on the regulation of medicines and medical devices. There are currently eight such committees: [citation needed] Advisory Board on the Registration of Homeopathic Products; Herbal Medicines Advisory Committee; The Review Panel

  4. Marketing Authorisation Application - Wikipedia

    en.wikipedia.org/wiki/Marketing_authorisation...

    Marketing Authorisation Application (MAA) is an application submitted by a drug manufacturer seeking marketing authorisation, that is permission to bring a medicinal product (for example, a new medicine or generic medicine) to the market.

  5. MHRA - Wikipedia

    en.wikipedia.org/wiki/MHRA

    Download as PDF; Printable version; In other projects Wikidata item; ... MHRA may refer to: Organisations. Medicines and Healthcare products Regulatory Agency, UK;

  6. List of stringent regulatory authorities - Wikipedia

    en.wikipedia.org/wiki/List_of_stringent...

    A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...

  7. European Medicines Agency - Wikipedia

    en.wikipedia.org/wiki/European_Medicines_Agency

    More specifically, it coordinates the evaluation and monitoring of centrally authorised products and national referrals, develops technical guidance and provides scientific advice to sponsors. Its scope of operations is medicinal products for human and veterinary use including biologics and advanced therapies, and herbal medicinal products .

  8. File:Bengali Letter A.svg - Wikipedia

    en.wikipedia.org/wiki/File:Bengali_Letter_A.svg

    Date/Time Thumbnail Dimensions User Comment; current: 01:07, 15 October 2018: 64 × 64 (4 KB): আফতাবুজ্জামান: Reverted to version as of 17: ...

  9. File:Bengali Letter Tta.svg - Wikipedia

    en.wikipedia.org/wiki/File:Bengali_Letter_Tta.svg

    Download QR code; In other projects ... Bengali Letter Tta. Date: 2 October 2010: Source: Own work: ... The copyright protection can be limited to the literary form ...