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Questions and Answers document regarding the Implementation of the new Manufacturer Incident Report (MIR) Form
Commission Guidelines on Union-wide derogations for medical devices
How to verify that medical devices and personal protective equipment can be lawfully placed on the EU market and thus purchased and used – also in the COVID-19 context
Changelog file 2020
MDCG 2020-10/1 Safety reporting in clinical investigations of medical devices under the Regulation (EU) 2017/745
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