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Webinar
Medical Devices

Clinical Masterclass Series 2022 Post Market Clinical Follow Up Under MDR

The medical device regulations specifically state that post-market clinical follow-up is a continuous process under the regulations.

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In this Webinar:

PMS and PMCF requirements: where are they defined?
Does PMCF under the MDR mean the same as PMCF under the directives?
Types and plans of PMCF.
PMCF Reports.

Post market clinical follow up under MDR

BSI interpretation of post market clinical follow up under the MDR.

Richard Holborow, Head of Clinical Compliance, BSI

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