Скачать или смотреть IRB (Institutional Review Board) | IEC (Independent Ethics Committee) | Regulatory Affairs

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The Institutional Review Board (IRB) / Independent Ethics Committee (IEC) plays a critical role in safeguarding the rights, safety, and well-being of participants in clinical trials. These committees ensure that research is conducted ethically and in compliance with regulatory guidelines. In this video, we’ll explain the functions of IRB/IEC, their approval process, and how they protect human subjects in clinical research.

What You’ll Learn:

• What IRB (Institutional Review Board) and IEC (Independent Ethics Committee) are.
• The key roles and responsibilities of IRB/IEC in clinical trials.
• How IRB/IEC reviews and approves research protocols to ensure ethical compliance.
• Regulatory guidelines governing IRB/IEC (ICH-GCP, FDA, EMA, CDSCO).
• The importance of informed consent and patient protection in clinical research.

This video is essential for pharmacy students, clinical researchers, and regulatory professionals who want to understand how ethical oversight is maintained in clinical trials.

If you find this video informative, don’t forget to like, comment, and share it with your peers to spread awareness about the importance of IRB/IEC in clinical research!

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