Amy Dow

Amy Dow

Epstein Becker & Green

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FDA and OHRP Issue Joint Draft Guidance on Content, Organization, and Presentation of Consent Forms for Research Participants

On March 1, 2024, the U.S. Food and Drug Administration (FDA) and the U.S. Department of Health and Human Services’ (HHS’s) Office for Human Research Protections (OHRP) released a draft guidance titled “Key Information and...more

3/19/2024  /  Clinical Trials , Department of Health and Human Services (HHS) , Food and Drug Administration (FDA) , Medical Research , Office for Human Research Protections (OHRP)
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