13 principles of ICH GCP - Good Clinical Practices Guidelines in Clinical Research #gcp #ich

ICH - Good Clinical Practices play critical role in conducting clinical trials in ethical and scientifically sound manner. These guidelines are crucial to understand as it lays fundamentals of clinical research methodology and global ethical and scientific quality standards.

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In this video we talk about:
(0:00) Intro
(0:37) What is ICH - Good Clinical Practices (GCP)
(2:30) Principle 1 - Ethics in Clinical Trials
(3:49) Principle 2 - Risk vs Benefits of Clinical Trials
(4:58) Principle 3 - Trial participants and Safety
(5:56) Principle 4 - Information on Medicinal Products
(7:04) Principle 5 - Good Quality Trials
(7:44) Principle 6 - Compliance with Study Protocol
(8:58) Principle 7 - Medical Decision and Responsibilities
(9:34) Principle 8 - Trial staff competency
(10:15) Principle 9 - Informed consent in Clinical Trials
(11:04) Principle 10 - Clinical Trial Data
(11:42) Principle 11 - Confidentiality in Clinical Trials
(12:36) Principle 12 - Good manufacturing Practices
(13:17) Principle 13 - Quality Assurance in Clinical Trials
(14:23) Advanced certification in Clinical Research

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[snehaldongare]

Thanks a lot, I have my interview tomorrow for clinical trial transparency associate ; this really helps me i hope

[rp]

Thank You. I am from medical background und currently doing a CRA course in a German Language. So for me it's really helpful to understand first all of in english.

[sammyjeff]

Thanks man. with the help of your video I was able to just refresh my knowledge

[manojSitalgera]

Thank you i learned something new from u

[sagarahire]

Thank you sir i little bit confused in ICH full form
It's International Conference on Hormonization or International Council for Hormonization.

[gayatripai]

Hi
May i know what software knowledge should we have to get into different levels of pharma .