In the nine months since the UK voted to leave the EU, the European Medicines Agency has been working out how best to deal with two key issues: whether, and how, the UK regulator, the MHRA, might continue to work with or within the EU drug regulatory system, and the challenges posed by the EMA’s forced relocation to one of the remaining 27 EU member states.
The EMA’s planning has been underpinned by the establishment of an Operational Relocation Preparedness (ORP) task force at the EMA,...
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