CCRA Practice Questions - ACRP Certified Clinical Research Associate Exam

What is the PRIMARY purpose of informed consent in a clinical trial?

To protect the sponsor from legal liability To ensure the subject voluntarily agrees to participate after understanding the trial's purpose, procedures, risks, and benefits To fulfill a regulatory requirement with no direct impact on the subject To allow the investigator to enroll subjects more quickly

Correct Answer:

To ensure the subject voluntarily agrees to participate after understanding the trial's purpose, procedures, risks, and benefits

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