CDSCO Releases Draft Guidelines for Clinical Trials in INDIA [Video]

In this video we look into the latest draft guidelines released by the CDSCO and understand the key focus areas that impact the clinical trial and pharma industry as well as policy improvements and mandates proposed by the CDSCO in this guidelines.

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⚠️ Links to most helpful videos ⚠️

NDCT Rules 2019: https://youtu.be/HFn90huWhmc
SAE reporting and SUGAM: https://youtu.be/DkcwW1LXdgg
Adverse events (AE) in Clinical Trials: https://youtu.be/GsqSn7asibk
CRA Interview: https://youtu.be/r-5PNfEHWrI
CRC interview: https://youtu.be/zM78E5BNud4
Clinical Research Coordinator: https://youtu.be/2QNRFv7CzzU
Clinical Research explained under 5 mins: https://youtu.be/CXSh1Zf2ZME
13 Principle of ICH-GCP: https://youtu.be/TCW55krWzb4
CRC or CRA: https://youtu.be/t9iVOm2WivM
Phases of Clinical trials: https://youtu.be/HcscuxWOSCM
Good Clinical Practices (ICH-GCP): https://youtu.be/ugumBwwbuGw
Ethics Committee in Clinical Research: https://youtu.be/nrOkRQjtInI

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In this video, We explain about:

(0:00) Intro
(0:45) CDSCO releases draft guidelines
(1:50) Key Focus Areas
(5:18) What does sponsor needs to know?
(9:20) Guideline Impact