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.

Speakers

Hear from the experts in this webinar

Speaker

Richard Holborow

Head of Clinical Compliance, BSI

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