20 Sep 2022

Minimize Risks to Special Populations in Clinical Trials

Advise healthcare clients on key regulatory and compliance considerations for clinical trials involving so-called special populations of research subjects like pregnant women, human fetuses, neonates, prisoners, and children. Understand how the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) set standards to protect these populations from undue influence when serving as research subjects in clinical trials.

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