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Tag Archives: PMCF

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PMCF Planning as per EU MDR

As the Medical Device Regulation (MDR) deadlines are approaching for re-certification and/or introduction of new products, manufacturers are also working to start or fulfil the Post-market Clinical Follow-up (PMCF) activities as per requirements set out in Annex XIV, part B of the MDR.

August 27, 2020Clinical TrialsBy Namrata Singh
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