Filtres
Regulatory Update: Microplastics and Medical Devices
Electronic instructions for use for medical devices
Labelling requirements for medical devices under the new EU Product Safety Regulation
Medical device manufacturers: control your supply chain for MDR and IVDR requirements
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
Updated post-market surveillance (PMS) rules for medical devices in the UK: differences from the EU regulations
GB International recognition for medical devices
Higher Administrative Court of Münster: Subsequent authorization of a homeopathic medicinal product
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
Medical devices in the context of the European Commission's AI Regulation draft
Making sense of timelines and certificate extensions for placing medical devices on UK and EU markets