The upcoming IVDR regulation will be fully applicable as of May 26, 2022. This will imply several changes in the In-Vitro Diagnostics regulatory landscape, and manufacturers must make sure to be compliant on time, in order to keep selling their devices on the European market.
In this webinar, we will provide an overview of:
- New classification rules under the IVDR
- Special topics: HSC list, EC database, National Derogation lists