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GCP/ICH Obligations of Investigators Conducting Clinical Trials

This course addresses obligations of investigators as described by the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH).

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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.

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Duration

60 minutes

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Library

Clinical: Pharmaceutical

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Functional area

Clinical and Quality

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ComplianceWire

ComplianceWire Online and Custom Content Brochure

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ComplianceWire

ComplianceWire Life Sciences eLearning Offerings

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