Question: When would an IRB consider the risks of a study to be controlled? When the risks of harm are unacceptable. When there is an appropriate

When would an IRB consider the risks of a study to be controlled? When the risks of harm are unacceptable. When there is an appropriate plan to remove all risks of harm. When risk mitigation strategies only consider harms encountered in daily life. When there is an appropriate risk mitigation and management plan

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