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Good Clinical Practice - ICH Guidelines E6 R2
time3-4hrs
timeadvanced level
Clinical research involving human subjects is a very sensitive matter requiring careful decision-making by those involved. The ICH guidelines to good clinical practice allow researchers to conduct clinical trials with the correct methodologies. By completing this course, clinical research aspirants can gain detailed insight into conducting fruitful clinical research while ensuring the safety of all those involved. ㅤㅤㅤㅤ
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Good Clinical Practice - ICH Guidelines E6 R2
Gain critical information about good clinical practice (GCP) in conducting safe clinical trials in this free course.
Clinical research involving human subjects is a very sensitive matter requiring careful decision-making by those involved. The ICH guidelines to good clinical practice allow researchers to conduct clinical trials with the correct methodologies. By completing this course, clinical research aspirants can gain detailed insight into conducting fruitful clinical research while ensuring the safety of all those involved. ㅤㅤㅤㅤ
checked1Course description
checked1Course module
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Module 1
5 Lessons
An Introduction to ICH and GCP
This module introduces you to the International Council for Harmonization and its Efficacy Guideline E6, which is dedicated to Good Clinical Practice (GCP) principles. You will learn about ICH's mission, working groups, and principles for GCP. The module also explains requirements concerning the role of IRBs and IECs in clinical trials.
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1.Learning Outcomes
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2.Principals to ICH
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3.Principles and Practices of ICH GCP
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4.Role and Responsibilities of IRBs in Clinical Trials
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5.Lesson Summary
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Module 2
6 Lessons
GCP Essentials for a Clinical Trial
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Module 3
1 Lessons
Course assessment
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