Pharmaceutical, food and medical devices companies that market their products and services in Europe face an intricate web of rules and regulations. EU regulation is continually evolving: it is adopted in Brussels, applied by European and national administrations and interpreted by the European and national courts. In order to ensure compliance, companies need up-to-date, practical advice on how the EU rules affect their industry.
Sidley’s EU life sciences lawyers provide integrated legal services that encompass the entire spectrum of corporate, transactional, litigation and government matters. We have substantial experience addressing a wide variety of regulatory and market access issues related to pharmaceuticals, biotechnology, medical devices, cosmetics, food and food supplements.