Publications

Labelling requirements for medical devices under the new EU Product Safety Regulation

par Christoph Behm

Life sciences M&A roundup: August 2024

par Ross McNaughton et Sarah Cole

Life sciences M&A roundup: July 2024

par Ross McNaughton et Sarah Cole

Life sciences M&A roundup: June 2024

par Ross McNaughton et Sarah Cole

Supply chain control: what medical device manufacturers need to know

par Alison Dennis et Paolo Palmigiano

Medical device manufacturers: control your supply chain for MDR and IVDR requirements

par Alison Dennis et Paolo Palmigiano

Medical device manufacturers and your Approved Body

What to do in the light of new case law if you consider your notified body has made a wrong decision

par Julian Randall et Alison Dennis

GB International recognition for medical devices

par Alison Dennis

Higher Administrative Court of Münster: Subsequent authorization of a homeopathic medicinal product

par Dr. Daniel Tietjen

Artificial Intelligence (AI) in medical devices: The better the product, the harder the conformity assessment?

Legal requirements for green claims in advertising for medical devices

par Dr. Daniel Tietjen

Medical devices in the context of the European Commission's AI Regulation draft

par Dr. Stefanie Greifeneder