medicines

Medicines and Healthcare Products Regulatory Agency

The Medicines and Healthcare Products Regulatory Agency (MHRA) is an executive agency of the Department of Health. It licenses and monitors medicines and reviews their advertising. Its website provides information about the work of the MHRA; it includes regulatory guidance, regulations, EU directives, consultation documents, newsletters and reports. Topics covered include the licensing of medicines; the licensing and regulation of herbal medicines; the regulation of medical devices; the regulation of nanotechnology; and clinical trials of medicines.

Research guide on TRIPS and compulsory licensing:access to innovative pharmaceuticals for least developed countries

Online guide focusing on the legal and economic factors preventing poorer countries gaining access to innovative drugs, by patent attorney Do Hyung Kim. Pubished on New York University's Globalex website and updated periodically, it gives background information about the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) and looks at the problems of compulsory licensing, such as the risks of arbitrage and counterfeit drugs.

Subscribe to medicines