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UUSOP - 8 (OBTAINING WRITTEN INFORMED CONSENT) is a Course

UUSOP - 8 (OBTAINING WRITTEN INFORMED CONSENT)

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The Principal Investigator (PI) of a clinical research study is responsible to ensure that all human subjects provide voluntary informed consent before participating in the study. Informed consent is an ongoing process that begins at the first contact with a prospective subject and continues throughout their participation. The PI may delegate the task of conducting informed consent to qualified sub-investigators or study staff.

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