The EC releases update on MDR-IVDR applications and certification
The European Commission’s (EC’s) Directorate-General for Health and Food Safety recently published a survey of notified bodies. This was conducted between April and May 2023, eliciting responses from all 39 notified bodies designated under the Medical Devices Regulation (MDR) and 10 Notified bodies designated under the In Vitro Diagnostic Regulation (IVDR).
European Commission Ec Directorate European Commission Food Safety Medical Devices Regulation Vitro Diagnostic Regulation Amending Regulation
Source: bioworld.com