What’s NEW in ICH GCP E6 R(3) Guideline? Key Changes & Implications for Clinical Researchers

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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 Questions & Answers: A Compl...  
Clinical Research explained under 5 mins:    • 5 minute Crash Course in Clinical Research...  
13 Principle of ICH-GCP:    • 13 principles of ICH GCP - Good Clinical P...  
Nuremberg Code:    • Nuremberg Code and Nazi doctor trials -   ...  
Thalidomide Tragedy:    • The Thalodomide Tragedy - Clinical Researc...  
Tuskegee Syphilis Study:    • Tuskegee Syphilis Study & Belmont Report -...  
Phases of Clinical trials:    • What are Phase trials? - Explaining all Ph...  
Good Clinical Practices (ICH-GCP):    • Good Clinical Practices (GCP) and 13 Princ...  
Ethics Committee in Clinical Research:    • Ethics committee in Clinical Research  
NDCT Rules 2019:    • New Drugs and Clinical Trials Rules, 2019 ...  
SAE reporting and SUGAM:    • Serious Adverse events & SAE reporting - W...  
Adverse events (AE) in Clinical Trials:    • Adverse Events & Adverse Drug reactions in...  



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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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