Principles of ICH GCP
According to ICH GCP Section 2: The Principles of GCP which of the following is not one of the 13 stated priniciples?
Freely given informed consent should be obtained from every subject prior to clinical trial participation.
The standard treatment of trial subjects should not be inhibited by inclusion in a clinical trial
The available nonclinical and clinical information on an investigational product should be adequate to support the proposed clinical trial.
The rights, safety, and well-being of the trial subjects are the most important considerations and should prevail over interests of science and society.
Learning Management Centre
My GCP Zone Login
Retrieve Online Order
PharmaSchool Online Courses:
Click here for the full range of Online GCP, Clinical Research and Development Courses from PharmaSchool.
Users in the following countries:
News & Corporate Information
Terms & Conditions