Maurits J F Lugard

Practice Areas

Maurits Lugard leads Sidley’s Life Sciences team in Brussels, a part of Sidley’s premier Global Life Sciences group. Maurits has an uncommon wealth of experience in EU law, drawing on his tenure within the European Commission and on years of private practice in the regulatory capitals of Brussels and Washington, D.C.

Maurits’ practice focuses on helping clients navigate the complex web of EU and Member State rules and procedures with an emphasis on food, drugs, medical devices, cosmetics and biotechnology. He helps corporate clients and trade associations shape future legislation and advises on the complex legal issues of the current regulations in areas such as pharmacovigilance (drug safety), clinical trials, marketing authorizations, advertising and promotional issues, labeling and the application of the precautionary principle.

Maurits also advises clients on a broad range of market access and product safety issues such as GMP compliance, life-cycle management, product recall procedures, adverse events, health claims, in-vitro diagnostics, implantable medical devices, food additives, parallel trade and supply chain management. He also advises on pharmaceutical contractual issues, including distribution, supply, manufacturing, R&D and other cooperation agreements in Europe. He has represented clients in matters before the European Commission, the European Medicines Agency, the European Food Safety Authority and Member State authorities.