Good Clinical Practice for Clinical Research Professionals
Complete, Certified ICH GCP E6 (R2+R3) Course for Investigators, Study Coordinators, Sponsors, Monitors and Study staff
4.44 (1176 reviews)
2 926
students
3.5 hours
content
Nov 2024
last update
$64.99
regular price
What you will learn
Identify and understand the ICH-GCP requirements throughout the conduct of clinical trials
Learn the core principles of ICH-GCP R2 and R3 and how to implement them in practice
Define the roles and responsibilities of each involved key stakeholder: Ethics Committees, Sponsors and Investigators
Understand the purpose of the essential documents and the best practice for filing in the TMF
Understand the essential requirements and contents of the Investigator's Brochure and the Protocol
Practice on real cases: Identify common ICH-GCP inspection findings (FDA warning letters) and how to avoid them
Practice on real cases: Conduct a gap analysis in your organization based on a real MHRA inspection report
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4701910
udemy ID
24/05/2022
course created date
03/07/2022
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