Skip to main content
  • Training

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).

A group of five work co-workers review professional document in a medical setting

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.

icon of a clock

Duration

60 minutes

icon of a gear rotating

Library

Clinical: Pharmaceutical

icon of a book

Functional area

Clinical and Quality

Downloads
ComplianceWire

ComplianceWire Online and Custom Content Brochure

810.34 KB
ComplianceWire

ComplianceWire Life Sciences eLearning Offerings

2.73 MB
X

Get connected with our sales team

Thanks for your interest in our products and services. Let's collect some information so we can connect you with the right person.

Please wait…