Alexander Wenzel

Supervising Associate at Simmons & Simmons LLP

Speaker

Alexander is a trusted advisor who guides Life Sciences companies through the intricate landscape of EU regulation. He assists global and emerging companies with navigating the regulatory and technical regulatory requirements applicable to the CE marking of medical devices, while seamlessly integrating expertise in product safety requirements with data protection requirements.

The scope of his practice covers all life cycles of (in vitro) medical devices, (advanced therapeutic) medicinal products and digital health products. He advises clients on all regulatory aspects governing their product including classifications, clinical trials and investigations, GCP and GMP, regulatory market exclusivities, marketing authorization applications and conformity assessment procedures.

He became a member of the Brussels Bar in 2018. Prior to joining Simmons & Simmons in 2023, Alexander trained with the enforcement coordination unit of the European Commission’s DG GROW and practiced law at two global law firms.