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.
Link to the important videos:
Nuremberg Code: [ Ссылка ]
Thalidomide Tragedy: [ Ссылка ]
Tuskegee Syphilis Study: [ Ссылка ]
Phases of Clinical trials: [ Ссылка ]
Good Clinical Practices (ICH-GCP): [ Ссылка ]
Ethics Committee in Clinical Research: [ Ссылка ]
NDCT Rules 2019: [ Ссылка ]
SAE reporting and SUGAM: [ Ссылка ]
Adverse events (AE) in Clinical Trials: [ Ссылка ]
For queries/ contact please reach out at below mentioned platforms
Contact: 83900 88032 / 81778 96079
To Register, please click on the link below:
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Instagram ID: clinical_aim_research
Gmail: clinicalaimresearch@gmail.com
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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