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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
Regulating AI as a medical device in the UK
IVDR extended transition period: What it means for IVD manufacturers
The CJEU: The recurring question of the separation of medicinal products and medical devices
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
MHRA response to consultation on UK regulation of medical devices
