Description
This course addresses the obligations of investigators as described by The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). It focuses on the investigator's responsibilities to protect the rights and welfare of human subjects. By extension, these responsibilities also apply to other investigation site staff involved in the planning, conduct, recording and reporting of clinical trials.
Duration
60 minutes
Library
Clinical: Pharmaceutical
Functional area
Clinical and Quality
ComplianceWire Online and Custom Content Brochure
810.34 KB
