Webinar
Medical Devices

Claiming Equivalence Under the MDR – Regulatory Considerations

Reviewing MDR Requirements, General principles of Equivalence under the MDR and Regulator aspects of Equivalence based on classification.

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This webinar:

General principles of Equivalence under MDR.
Regulatory aspects of Equivalence based on classification.
Clinical data for Equivalent devices.
Similar devices.

Speakers

Hear from the experts in this webinar

Speaker

Richard Holborow

Head of Clinical Compliance, BSI

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