Coordinating investigator signature of clinical study reports

Current effective version

PDF iconAdopted guideline

Reference numberCPMP/EWP/2747/00
Effective from01/04/2002
KeywordsCo-ordinating investigator, protocol, clinical study report, multicentre studies
DescriptionThis document provides guidance on the designation of the coordinating investigator who will sign clinical study reports for multicentre studies.

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