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From course:

DRUG DISCOVERY DEVELOPMENT (DDD)

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Question:

A CRITICAL ADMINISTRATIVE ELEMENT in all institutions in which HUMAN RESEARCH IS BEING DONE. Has the AUTHORITY TO EXAMINE AND ANALYZE the PROTOCOL OF ANY RESEARCH PROPOSAL involving human subjects to ensure that such research correctly balances the potential benefits against risks to which the subject will be exposed and to specify what information must be presented to the subject before he or she can be said to have given informed consent.

Author: LEIGHTON DWIGHT OBILLOS



Answer:

The Institutional Review Board (IRB)


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