In clinical research conducted in the UAE, what regulatory body must approve a human subject study prior to participant enrollment?

Answer and explanation

Correct answer: D. An authorized Institutional Review Board or Research Ethics Committee

Answer: An authorized Institutional Review Board or Research Ethics Committee.
Why not the others: Research on human subjects requires formal ethical review and approval by an accredited Institutional Review Board (IRB) or Research Ethics Committee (REC) to protect patient rights and welfare; Police, sales representatives, and trade licensing offices have no authority over clinical research ethics.

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