MHRA

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MHRA

Medicines and Healthcare Regulatory Authority. An executive agency of the UK Department of Health which is responsible for ensuring that medicines and medical devices work, and are acceptably safe. It was created in 2003 from the merger of the Medicines Control Agency and the Medical Devices Agency.
References in periodicals archive ?
The Medicines and Healthcare products Regulatory Agency (MHRA) will be created from April 2003 from a merger of the Medicines Control Agency and the Medical Devices Agency.
Reclassification of Nexium Control 20mg Tablets announced by the Medicines and Healthcare products Regulatory Agency today (27 January 2014).
NASDAQ:SLXP) today announced that the Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorization for Diacol[TM] 1500 mg Tablets in the United Kingdom.
Taro," NASDAQ: TARO) reported today that Taro Pharmaceuticals (UK) Limited ("Taro UK"), its affiliate in the United Kingdom, has been granted a marketing authorization for Etopan XL Tablets 600 mg, Etodolac ("Etopan XL") by the Medicines and Healthcare Products Regulatory Agency, the UK equivalent of the U.