Protection of human subjects; informed consent--FDA. Final rule.

  • Published 1996 in Federal register

Abstract

The Food and Drug Administration (FDA) is amending its current informed consent regulations to permit harmonization of the Department of Health and Human Services' (DHHS) policies on emergency research and to reduce confusion on when such research can proceed without obtaining an individual subject's informed consent. This regulation provides a narrow… (More)

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@article{1996ProtectionOH, title={Protection of human subjects; informed consent--FDA. Final rule.}, author={}, journal={Federal register}, year={1996}, volume={61 192}, pages={51498-533} }