Latest thinking

 

Latest thinking

Brexit Bulletin: marketing authorisations for centrally-authorised medicinal products post Brexit

26 June 2017

Industries: Life Sciences and Healthcare

On 31 May 2017, the European Commission and the European Medicines Agency (EMA) published a list of Q&A “related to the United Kingdom’s withdrawal from the European Union with regard to the medicinal products for human and veterinary use within the framework of the Centralised Procedure” (“the Q&A document”).

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