Participant IMP-IMD Accountability Log. Logs/Templates and instructions for use - The Swiss Clinical Trial Organisation - SCTO

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Participant IMP-IMD Accountability Log. Logs/Templates and instructions for use

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Monitoring | Human Research Act - HRA | Quality Documents

Tracks receipt, dispensing, and return of Investigational Medicinal Product/Device. Ensures accurate accountability at both site and participant levels.

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Downloadable Documents:

SCTO MON tem 7bDownload DOCX (1.29 MB)SCTO MON tem 7b IFUDownload PDF (54.38 KB)