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Each IRB will evaluate the studys ethics (informed consent process, risk/benefit, etc.) and often wants to see the same core documents (protocol, IB, consent forms, investigator qualifications)

Dipak Kumar Sahoo, [email protected] Disclaimer All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers

Side effects may become noticeable at 0.6 mg, particularly nausea, reduced appetite, and gastrointestinal changes

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To qualify for Ozempic, you need to have a diagnosis of type 2 diabetes