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Webinar
Medical Devices
Preparing a Clinical Evaluation Report (part 1)
Preparing a good quality clinical evaluation report for submission to the notified body is vital to ensure they understand your device.
In this Webinar:
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Documenting the Device Description.
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Documenting Equivalence.
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Documenting Similar Devices Data.
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Documenting Clinical Claims.
Preparing a good clinical evaluation report (CER) for submission
This session will look how best to document the contents of a CER and this first session in the two part series.
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Richard Holborow, Head of Clinical Compliance, BSI
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Adam Liddle, Head of Life Sciences- Regulatory & Policy, BSI
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