News - January 10, 2019

Invitation – Inside the Minds of Regulators: Perspectives on EU Pharmaceutical & Medical Devices Law

EUCOPE, in collaboration with its member Sidley, as well as Navitas and PWC, is organising a conference on the 21st of February in Brussels, to discuss recent developments in pharma and medical devices law.

The event will bring together senior and former members of the European Commission, the European Medicines Agency (EMA), the Dutch Medicines Evaluation Board, the Swiss Agency for Therapeutic Products (Swissmedic), the U.S. Food & Drug Administration (FDA) as well as representatives from the regulatory and business community to address key issues of relevance to pharmaceutical and medical device companies in 2019.

Panel discussions will cover clinical trials, pharmacovigilance, orphan drugs, new pathways to marketing authorizations, falsified medicines, pharmaceutical incentives, transparency on pricing, pharmacy compounding, advanced therapy medicinal products (ATMPs), fees, off-label use, biosimilars, medical devices and Brexit.

This year’s keynote address will be presented by the European Commission’s Head of Unit to the Directorate General for Health and Food Safety (DG SANTE), Olga Solomon.

Click here to view the agenda and to register.