General Considerations ICH E8 (R1) for Clinical Studies

Complete Training Integrated into ICH GCP E6(R3) to Proactively Design Quality into Clinical Trials and Drug Development
3.70 (5 reviews)
Udemy
platform
English
language
Science
category
General Considerations ICH E8 (R1) for Clinical Studies
11
students
2.5 hours
content
Oct 2024
last update
$19.99
regular price

What you will learn

Understand the General Quality Principles of Clinical Research

Understand why a revision to the original E8 was needed

Understand the link between ICH E8 and ICH-Good Clinical Practice (GCP) E6 (R3)

Learn how to identify Critical to Quality (CtQ) factors

Identify and understand the ICH E8 requirements for optimal design and conduct clinical studies

Learn and understand how to apply the process to implement good design quality into clinical studies

Learn how to utilize good study design practice to optimize drug development planning

Understand the key elements of the study protocol that may be used to optimize the design of a study

Learn from the experience in case studies where Quality-by-Design (QbD) was implemented Vs not implemented

Screenshots

General Considerations ICH E8 (R1) for Clinical Studies - Screenshot_01General Considerations ICH E8 (R1) for Clinical Studies - Screenshot_02General Considerations ICH E8 (R1) for Clinical Studies - Screenshot_03General Considerations ICH E8 (R1) for Clinical Studies - Screenshot_04
Related Topics
4808620
udemy ID
7/31/2022
course created date
5/26/2023
course indexed date
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course submited by
General Considerations ICH E8 (R1) for Clinical Studies - | Comidoc