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List of words and phrases that will cause a veterinary product to be medicinal by presentation either through use or contextual use.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Defence Medical Services awards £2.5 million contract to Avenue3 for Project Mercury, enabling secure military medical records access worldwide.
MHRA’s mechanism for evaluating the justifications supplied by applicant organisations who plan to utilise decentralised manufacture.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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