Article R5211-36-2
Implantable medical devices, active implantable medical devices and class III devices must be subject to clinical investigations, unless the use of existing clinical data can be duly justified.
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Showing 7911–7920 of 38229 articles for “Art. R 134-6”
Implantable medical devices, active implantable medical devices and class III devices must be subject to clinical investigations, unless the use of existing clinical data can be duly justified.
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In the light of the investigation file and the opinions expressed, the Prefect entrusts the Director General of the Regional Health Agency with drawing up a summary report on the request and the resul…
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