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

Insights & Media

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Informatie en media

EU MDR – Post Market Clinical Follow-Up

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Annex XVI - Devices Without an Intended Medical Purpose

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Using Standards to Demonstrate Conformity

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Unlocking the Potential of Consumer Wearables in Healthcare

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Medical Device Lifetime - Assisting manufacturers

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Symbols & Details Required for Medical Devices & IVDs

Lees het whitepaper

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