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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 ...
Download QR code; Print/export ... Financial regulatory authorities of the United Kingdom (1 C, 6 P) L. ... Office for Nuclear Regulation;
In this list of financial regulatory and supervisory authorities, central banks are only listed where they act as direct supervisors of individual financial firms, and competition authorities and takeover panels are not listed unless they are set up exclusively for financial services.
The Government of the United Kingdom is divided into departments that each have responsibility, according to the government, for putting government policy into practice. [1] There are currently 24 ministerial departments, 20 non-ministerial departments, and 422 agencies and other public bodies, for a total of 465 departments. [2]
Executive agencies of the United Kingdom government (5 C, 42 P) Government bodies based in London (10 P) Government-owned companies of the United Kingdom (10 C, 33 P)
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
Local Government Act 1929; London Government Act 1963; Redcliffe-Maud Report (1969) Local Government Act 1972; Streamlining the cities (1983) Local Government Act 1985; Local Government Act 1988; Local Government etc. (Scotland) Act 1994; Local Government (Wales) Act 1994; Greater London Authority Act 1999; Local Government Act 2000 (applies to ...
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 ...