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Medicines and medical devices in the EU Single Market: Dreams and Reality

This conference will address the free movement of goods in the context of the European Single Market. The program will examine whether and to what extent a genuine Single Market exists for medicinal products and medical devices, both currently being heavily regulated at the EU and national level to ensure patient safety. The topic will be discussed from different angles, including parallel trade, the new regulations on medical devices, the new Clinical Trials Regulations, the Falsified Medicines Directive and, inevitably, Brexit. A mix of experienced legal practitioners and in-house counsel from across Europe will guide you through the rapidly changing life sciences regulatory landscape and bring you up to speed with the latest developments in the life sciences sector.

The academic program will be complemented by a rich social schedule. One of the speakers on the subject "The new Clinical Trials Regulation" and moderator will be our partner Jan Henning Martens.

Date and location:
27th - 29th June 2019, Zurich

For further information, please click here.

Jan Henning Martens

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