MHRA

Medicines and Healthcare products Regulatory Agency

MHRA 🇬🇧 United Kingdom National Active
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About

MHRA regulates medical devices in the United Kingdom following Brexit. It oversees device registration, UKCA marking, market surveillance, yellow card vigilance reporting, and clinical investigations.

Regulatory Details

Regulatory FrameworkUK MDR 2002 (as amended post-Brexit)
Device ClassificationClass I, Class IIa, Class IIb, Class III
Jurisdiction TypeNational
Country🇬🇧 United Kingdom
StatusActive

Contact Information

Country🇬🇧 United Kingdom
Address10 South Colonnade, Canary Wharf, London E14 4PU, UK
Phone+44-20-3080-6000

Official Website

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