British regulatory guidelines

The Medicines and Healthcare products Regulatory Agency (MHRA) is a government body which was set up in 2003 to bring together the functions of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA). These include the regulation of medicines and medical devices and equipment used in healthcare and the investigation of harmful incidents. The MHRA now also looks after blood and blood products, working with UK blood services, healthcare providers, and other relevant organisations to improve blood quality and safety.These include the regulation of medicines and medical devices and equipment used in healthcare and the investigation of harmful incidents. The MHRA now also looks after blood and blood products, working with UK blood services, healthcare providers, and other relevant organisations to improve blood quality and safety.

Related Journals of British regulatory guidelines

Clinical Research and Regulatory Affairs, Journal of Financial Regulation and Compliance, Brazilian Journal of Medical and Biological Research, European regulatory guidelines for biosimilars