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M3 - CE & Global Clinical Requirements - Post Market Clinical Follow Up for Medical Devices (QP)

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Part of Medical Devices QP Training Module 3

Dates: Thursday 16 to Friday 17 July 2025
Venue:
AMP Technology Centre, Sheffield
Cost:

£1470.00 excl VAT

Type: Medical Devices
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About this course

Within the European medical device directives there are specific requirements for obtaining post-market data relating to the clinical performance of your product utilizing a post market clinical follow-up plan. This course presents the requirements for PMCF and will enable you to understand the requirements and apply them to your internal procedures.

Who Should Attend

Development, regulatory and clinical personnel involved in the formulation of clinical investigations, evaluations and post market clinical follow-up of medical devices. The medical devices requirements are placing a major emphasis upon clinical data requirements for devices therefore programme managers, marketing and senior managers will also benefit from this module in that they will be able to understand the clinical requirements necessary for their devices and plan an appropriate commercialization strategy.

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