CAMD published FAQs to the transitional provisions of MDR and IVDR

bio_subbu

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The Competent Authorities for Medical Devices (CAMD) published 2 documents related to frequently asked questions (FAQ) to the transitional provisions of MDR and IVDR. These documents were developed by the CAMD Transition Subgroup (TSG) which was tasked with agreeing and providing greater clarity on the transition-related provisions in the new Regulations. For more details, refer CAMD website.

1. MDR Transition Provisions FAQ

2. IVDR Transition Provisions FAQ.
 
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