Скачать или смотреть Why India Must Follow ICH-GCP | NDCT 2019 Explained in Simple Terms

How do global clinical trial guidelines apply to India?
In this clip, we break down the relationship between NDCT 2019 — India’s regulatory framework — and ICH-GCP, the internationally accepted standard for clinical research.

You’ll learn:
✔ Why India MUST follow NDCT 2019
✔ Why global trials require ICH-GCP compliance
✔ How multi-country trials demand harmonized standards
✔ How these guidelines ensure data acceptance worldwide
✔ What this means for CR professionals, investigators & students

India’s clinical research ecosystem is expanding rapidly — but global acceptance depends on following internationally aligned regulations

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(clinical trial ethics, serious adverse event, SAE reporting India, Institutional Ethics Committee, IEC role clinical trials, adverse event compensation, clinical research India, regulatory guidelines India, investigator responsibilities, participant safety clinical trials
clinical research ethics, ethics committee India, serious adverse events, clinical trials India, Dr Murnalini Kalikar interview, Canvass Academy, ISCR ethics council, clinical research careers, regulatory affairs India, informed consent process, internships, early job search, placement strategy, clinical research careers, student mindset, job readiness, networking, Canvass Academy, professional growth, industry exposure)
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