Скачать или смотреть CITI Program Course Preview - ICH E6(R3): An Introduction

The course describes the ICH’s Guideline for Good Clinical Practice E6(R3). E6(R3) includes several updates from E6(R2). This video-based course examines how the changes affect the responsibilities of investigators, sponsors, and Institutional Review Boards (IRBs). It details changes to the principles of GCP and key terminology used in Annex 1. The course concludes with an exploration of Annex 2 and its application to emerging technologies and clinical trial designs.

Suggested Audiences: Academic Medical Centers, Biomedical Product Companies, Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Principal Investigators, Regulatory Agencies, Sponsors, Students

To learn more about this course, please visit: https://about.citiprogram.org/courses...