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  2. 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

  3. List of pharmaceutical manufacturers in the United Kingdom

    en.wikipedia.org/wiki/List_of_pharmaceutical...

    This is a list of manufacturers and suppliers of pharmaceuticals with operations in the United Kingdom.. Note: the activities of the parent companies of many of the companies listed below are not restricted solely to the United Kingdom.

  4. British Pharmacopoeia - Wikipedia

    en.wikipedia.org/wiki/British_Pharmacopoeia

    British Approved Names (BANs) are devised or selected by the British Pharmacopoeia Commission (BPC), and published by the Health Ministers, on the recommendation of the Commission on Human Medicines, to provide a list of names of substances or articles referred to in Section 100 of the Medicines Act 1968. BANs are short, distinctive names for ...

  5. 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 ...

  6. British Approved Name - Wikipedia

    en.wikipedia.org/wiki/British_Approved_Name

    A British Approved Name (BAN) is the official, non-proprietary, or generic name given to a pharmaceutical substance, as defined in the British Pharmacopoeia (BP). [1] The BAN is also the official name used in some countries around the world, because starting in 1953, proposed new names were evaluated by a panel of experts from WHO in conjunction with the BP commission to ensure naming ...

  7. Food and Drug Administration - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drug_Administration

    The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services.The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines ...

  8. Association of the British Pharmaceutical Industry - Wikipedia

    en.wikipedia.org/wiki/Association_of_the_British...

    The Association of the British Pharmaceutical Industry (ABPI) is the trade association for over 120 companies in the UK producing prescription medicines for humans, founded in 1891. [1] It is the British equivalent of America's PhRMA ; however, the member companies research, develop, manufacture and supply medicines prescribed for the National ...

  9. List of regulators in the United Kingdom - Wikipedia

    en.wikipedia.org/wiki/List_of_regulators_in_the...

    The following is a list of regulators in the UK. Regulators exercise regulatory or supervisory authority over a variety of endeavours. In addition, local authorities in the UK provide regulatory functions in a number of areas. Professional associations also act to regulate their memberships. The UK is also bound by a number of European and ...