Our attorneys have experience on, and can offer practical and strategic guidance in, many aspects of life sciences and “health law”.
We advise on regulatory requirements connected to a wide variety of issues, such as the commercialization of pharmaceutical products and medical devices, the performance of clinical trials, promotional activities for pharmaceutical products and medical devices, data protection compliance, commercial arrangements and anticorruption compliance.
Our life sciences clients range from pharmaceutical companies to medical device manufacturers, biotechnology companies, medical insurers, health IT providers and health care providers.
We are especially skilled in drafting and negotiating acquisition agreements, licensing and partnering agreements, clinical trials agreements, co-promotion and co-marketing agreements, research and development agreements.
We advise clients with respect to their public procurement issues, including litigation before administrative courts, we offer guidance on public-private partnerships and other administrative law issues.
We work closely with the Alliance of European Life Sciences Law Firms, of which our firm is a member.
We collect our reflections on legal issues relating to life sciences, innovation and healthcare on our blog: lawhealthtech.com.