What’s NEW in ICH GCP E6 R(3) Guideline? Key Changes & Implications for Clinical Researchers
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- เผยแพร่เมื่อ 14 มิ.ย. 2024
- Know all about the key changes and implications of the ICH GCP E6 R(3) revisions and what the future beholds for you as a clinical research professional.
Link to the important videos:
CRA Interview: • CRA Interview Question...
Clinical Research explained under 5 mins: • How to start a Career ...
13 Principle of ICH-GCP: • 13 principles of ICH G...
Nuremberg Code: • Nuremberg Code and Naz...
Thalidomide Tragedy: • The Thalodomide Traged...
Tuskegee Syphilis Study: • Tuskegee Syphilis Stud...
Phases of Clinical trials: • What are Phase trials?...
Good Clinical Practices (ICH-GCP): • Good Clinical Practice...
Ethics Committee in Clinical Research: • Ethics committee in Cl...
NDCT Rules 2019: • New Drugs and Clinical...
SAE reporting and SUGAM: • Serious Adverse events...
Adverse events (AE) in Clinical Trials: • Adverse Events & Adver...
For queries about Advanced Certification in Clinical Research, please reach out/contact at below mentioned platforms
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docs.google.com/forms/d/135mI...
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For any queries, kindly comment in the description box below.
In this video, We explain about:
(0:00) Intro
(1:14) ICH-GCP Fundamentals
(3:17) History of ICH-GCP guidelines
(4:36) Key Changes in E6 R(3) guidelines
(11:11) Impact of E6 R(3) guidelines
(15:30) Summary of E6 R(3) guidelines
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Thank you! Very helpful, easy to understand
Thank you so much for the video!!!
Glad it was helpful!
Thank you so much sir
Most welcome
Thanks for the video, is the ICH E6 R(3) implemented now?
Not yet but soon, since the FDA has recommended it will soon be ratified!
Why was the Belmont Report excluded?
Can you please mention the timestamp.in the video where this is mentioned?