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2. iPLEDGE program - Wikipedia

   en.wikipedia.org/wiki/IPLEDGE_program

   Though prescriber and pharmacy populations have become more familiar with the requirements of the iPLEDGE Program over the years, and some of the initial issues with the system have subsided, the nature of the restrictive distribution program continues to cause inconvenience, added expenses, and interruptions in the course of treatment. [20]

3. Medicines and Healthcare products Regulatory Agency

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

   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 Health Committee, [44] for having undergone regulatory capture, i.e. advancing the interests of the drug companies rather than the interests of the public.

4. Formulary (pharmacy) - Wikipedia

   en.wikipedia.org/wiki/Formulary_(pharmacy)

   Usage of the database is free of charge and it has no promotional texts or advertising. [15] FASS has been developed by the Swedish Association of the Pharmaceutical Industry (LIF) in close cooperation with Sweden's pharmaceutical industry , with additional assistance from the Medical Products Agency , the Pharmaceutical Benefits Board and the ...

5. Erythromycin/isotretinoin - Wikipedia

   en.wikipedia.org/wiki/Erythromycin/isotretinoin

   Isotretinoin is a pharmaceutical derivative of retinoic acid (a metabolite of vitamin A). Its mechanism of action is believed to involve reduction in the amount of sebum produced by sebaceous glands on the skin's surface.

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. Indian Pharmacopoeia Commission - Wikipedia

   en.wikipedia.org/wiki/Indian_Pharmacopoeia...

   Indian Pharmacopoeia Commission (IPC) is an autonomous institution of the Ministry of Health and Family Welfare which sets standards for all drugs that are manufactured, sold and consumed in India. [3]

8. 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]

9. MedDRA - Wikipedia

   en.wikipedia.org/wiki/MedDRA

   A subscription-based product of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), MedDRA or Medical Dictionary for Regulatory Activities is a clinically validated international medical terminology dictionary-thesaurus used by regulatory authorities and the biopharmaceutical industry during the regulatory process, from pre-marketing ...