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MHRA

The Medicines and Healthcare products Regulatory Agency (MHRA) are responsible for the regulation of medicines and medical devices and equipment used in healthcare, and theMedicines and Healthcare products Regulatory Agency investigation of harmful incidents. The Medicines and Healthcare products Regulatory Agency (MHRA) was set up in April 2003 from a merger of the Medicines Control Agency and the Medical Devices Agency. The MHRA is the government agency which is responsible for ensuring that medicines and medical devices work, and are acceptably safe. The MHRA is an executive agency of the Department of Health.