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MDR Annex XV (Clinical Investigations)

Clinical investigation requirements. Chapter I sets general requirements, Chapter II covers the documentation for the application for a clinical investigation, and Chapter III covers the sponsor's other obligations.

Chapters

Chapter I
General requirements
Chapter II
Documentation regarding the application for clinical investigation
Chapter III
Other obligations of the sponsor
Where it is written
Regulation (EU) 2017/745, Annex XV (consolidated text of 10 January 2025)
Also called
Annex XV, clinical investigation requirements

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