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The European Commission have recently released MDCG guidance (MDCG 2024-10) to help support the clinical evaluation of orphan devices.
You will gain an understanding of the MDCG guidance and will be aware of the process to apply to BSI with a device that qualifies to the criteria.
What defines a medical device as an Orphan Device (OD)?
What is expected of manufacturers?
Considerations and Limitations when documenting a Clinical Evaluation on Orphan Devices.
The Role of Pre-Clinical Data.
Head of Clinical Compliance, BSI
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