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Preparation for Brexit by marketing authorisation holders of centrally authorised medicinal products

The European Commission and the European Medicines Agency have issued a “Notice to marketing authorisation holders of centrally authorised medicinal products for human and veterinary use”, reminding marketing authorisation holders of centrally authorised medicines of their legal obligations in preparation for Brexit.

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#LegislationRegulatoryAffairs #MarketingAuthorizationHolders #Registrationprocedure

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