Resources - CAMD : CAMD

View and share our resources

Here you can find useful links and presentations from across the CAMD network, as well as publicly available outputs from the joint actions and working groups.

EC guidance: The role of medical devices

PIP Action plan

Medical devices - useful contacts

FAQs – IVDR Transitional provisions

FAQs - MDR Transitional provisions

MDR/IVDR Roadmap

Market surveillance of medical devices: Information for manufacturers

Market surveillance of medical devices: Information for notified bodies

Market surveillance of medical devices: Information for healthcare professionals

Improving how medical devices are checked and monitored across the EU: An intro for patients and consumers

EU Regulations for Medical Devices (MDR)

EU Regulations for in vitro Diagnostic Medical Devices (IVDR)