Bootcamp on the Development and Commercialization of Medicinal Products in Europe

This unique, one-day program is designed to provide U.S. lawyers with an overview of EU/UK biopharmaceutical regulation and compliance.

Please join our European life sciences team for an interactive program reviewing key topics relevant to the development and commercialization of medicinal products in Europe.

The European market offers substantial opportunities for U.S. companies, but also raises complex questions for product authorization and market access — addressing these questions early in the process can prevent delays, unsuccessful launches, and later compliance problems.

Whether you are new to the EU/UK regulatory frameworks for medicinal products or a veteran of the industry wanting a refresh, our leading European attorneys will walk you through the steps required to prepare for and execute a successful product launch. Learn firsthand from professionals who have helped companies large and small prepare to bring their products to the European market.

We will cover the evolving framework for the regulation of medicinal products in the EU and UK, key considerations for clinical development, and strategies for commercialization. We will also provide an overview of issues relevant to medical devices used with medicinal products, EU supply chain considerations, pricing and reimbursement, EU antitrust considerations, and the new product liability regime.

There will also be plenty of opportunities to ask the team questions.

We hope you can join us!