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.

Contributors

Claiming equivalence under the MDR – regulatory considerations

BSI’s understanding of claiming equivalence under the MDR and regulatory considerations.

Contributor
Richard Holborow

Head of Clinical Compliance, BSI.

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