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Ongoing work on ATMP GVP V update and transitional arrangements impact on the RMP document lifecycle update on RMP summaries publication GVP V updates expected impact on RMP life cycle. Information Day on Risk Management Planning and Post-Authorisation Studies 7 November 2016 European Medicines Agency London United Kingdom PROGRAMME COMMITTEE Enrica Alteri Head of the Human Medicines Evaluation Division EMA EU Peter Arlett Head of the Pharmacovigilance Department EMA EU Emil Cochino...
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