Artificial Intelligence (AI) in medical devices: The better the product, the harder the conformity assessment?
par Dr. Angela Knierim
Updated post-market surveillance (PMS) rules for medical devices in the UK: differences from the EU regulations
par Alison Dennis et Alice Matthews
Legal requirements for green claims in advertising for medical devices
par Dr. Daniel Tietjen et Sherin Sayed
Medical devices in the context of the European Commission's AI Regulation draft
par Sherin Sayed et Dr. Stefanie Greifeneder
Making sense of timelines and certificate extensions for placing medical devices on UK and EU markets
par Alison Dennis
Regulating AI as a medical device in the UK
par Alison Dennis et Nicholas Vollers
IVDR extended transition period: What it means for IVD manufacturers
The CJEU: The recurring question of the separation of medicinal products and medical devices
par Dr. Manja Epping et Sherin Sayed
To be, or not to be (a medical device): when does software qualify as a medical device?
Has the MDCG found the answer to the slow rate of MDR certifications?
Possibilities of special permissions for medical devices on national markets
par Dr. Daniel Tietjen
MHRA response to consultation on UK regulation of medical devices
© Taylor Wessing