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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. Rent regulation - Wikipedia

   en.wikipedia.org/wiki/Rent_regulation

   This is an accepted version of this page This is the latest accepted revision, reviewed on 23 February 2025. Regulations to reduce increases in housing rents "Rent control" redirects here. For other uses, see Rent control (disambiguation). Part of a series on Living spaces Main House: detached semi-detached terraced Apartment Bungalow Cottage Ecohouse Green home Housing project Human outpost I ...

4. Human Medicines Regulations 2012 - Wikipedia

   en.wikipedia.org/wiki/Human_Medicines...

   The Human Medicines Regulations 2012 in the United Kingdom were created, under statutory authority of the European Communities Act 1972 and the Medicines Act 1968 in 2012. The body responsible for their upkeep is the Medicines and Healthcare products Regulatory Agency. The regulations partially repealed the Medicines Act 1968 in line with EU ...

5. Rental agreement - Wikipedia

   en.wikipedia.org/wiki/Rental_agreement

   A rental agreement or lease may include a "rent review" clause which makes provision for the rental amount to be increased, the process for the landlord to provide notice of a rent increase and the options available to the tenant regarding acceptance or rejection of the proposed increase. [3]

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. Regulation of therapeutic goods - Wikipedia

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

   The role of therapeutic goods regulation is designed mainly to protect the health and safety of the population. Regulation is aimed at ensuring the safety, quality, and efficacy of the therapeutic goods which are covered under the scope of the regulation. In most jurisdictions, therapeutic goods must be registered before they are allowed to be ...