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  2. Product Licence Number - Wikipedia

    en.wikipedia.org/wiki/Product_Licence_Number

    products.mhra.gov.uk A Product Licence Number (or PL code for short) is a unique identifier on the packaging of medicines, used to uniquely identify the product. This code will normally remain the same despite the varying marketing and branding of the companies selling it.

  3. Medicines and Healthcare products Regulatory Agency

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

    In 2005, the MHRA was criticised by the House of Commons Health Committee for, among other things, lacking transparency, [41] and for inadequately checking drug licensing data. [42] The MHRA and the US Food and Drug Administration were criticised in the 2012 book Bad Pharma, [43] and in 2004 by David Healy in evidence to the House of Commons ...

  4. Marketing authorisation - Wikipedia

    en.wikipedia.org/wiki/Marketing_authorisation

    In most countries, a marketing authorisation is valid for a period of 5 years. After this period, one should apply for renewal of the marketing authorisation, usually by providing minimal data proving that quality, efficacy and safety characteristics are maintained and the risk-benefit ratio of the medicinal product is still favourable.

  5. Marketing Authorisation Application - Wikipedia

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

    A centralised marketing authorisation, issued by the European Commission, allows the holder to market a medicinal product throughout the European Economic Area (EEA), which comprises the EU Member States, Iceland, Norway and Liechtenstein. [2] In the United States, the equivalent process is called New Drug Application.

  6. Don't Buy Weight-Loss Medication From Unauthorized ... - AOL

    www.aol.com/finance/dont-buy-weight-loss...

    As the New Year begins, the U.K.’s Medicines and Healthcare Products Regulatory Agency (MHRA) is urging the public to avoid purchasing weight-loss medicines without a prescription from ...

  7. Regulation of therapeutic goods - Wikipedia

    en.wikipedia.org/wiki/Regulation_of_therapeutic...

    Medicines for Human Use in the United Kingdom are regulated by the Medicines and Healthcare products Regulatory Agency (MHRA). The availability of drugs is regulated by classification by the MHRA as part of marketing authorisation of a product. [citation needed] The United Kingdom has a three-tiered classification system: [citation needed]

  8. Reporting of vaccine side-effects should be mandatory – Tory ...

    www.aol.com/reporting-vaccine-side-effects...

    Esther McVey said there was a “gross underreporting” of the unintended impacts of vaccines, and said the Medicines and Healthcare products Regulatory Agency (MHRA) was in need of ...

  9. MHRA - Wikipedia

    en.wikipedia.org/wiki/MHRA

    Medicines and Healthcare products Regulatory ... Research Association, UK MHRA Style Guide, an ... Creative Commons Attribution-ShareAlike 4.0 License; ...