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close this bookGuidelines for good clinical practice (GCP) for trials on pharmaceutical products (WHO Technical Report Series, No. 850, 1995, Annex 3) (WHO, 1995, 36 p.)
close this folder8. RECORD KEEPING AND HANDLING OF DATA
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View the document8.1 Responsibilities of the investigator
View the document8.2 Responsibilities of the sponsor and the monitor
View the document8.3 Archiving of data