Emergency Medicine and the Development of the Food and Drug Administration's Final Rule on Informed Consent and Waiver of Informed Consent in Emergency Research Circumstances-Reference-Cited by-同舟云学术

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Emergency Medicine and the Development of the Food and Drug Administration's Final Rule on Informed Consent and Waiver of Informed Consent in Emergency Research Circumstances

Published:1998-04 Issue:4 Volume:5 Page:359-368
ISSN:1069-6563
Container-title:Academic Emergency Medicine
language:en
Short-container-title:

Author:

Biros Michelle H.,Runge Jeffrey W.,Lewis Roger J.,Doherty Christopher

Publisher

Wiley

Subject

Emergency Medicine,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1553-2712.1998.tb02722.x/fullpdf

Reference37 articles.

1. Protection of Human Subjects; Informed Consent and Waiver of Informed Consent Requirements in Certain Emergency Research:Final rules (21 CFR Part 50, et al., 45 CFR Part 46);Department of Health and Human Services;Fed. Reg.,21996

2. President apologizes:calls syphilis study ‘morally wrong;Shelton;Am Med News.,1997

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3. Misuse of “Usual Care” in Emergency Care Research: A Call for Adapting Rules Governing Exception from Informed Consent (EFIC) Studies;The American Journal of Bioethics;2020-01-02

4. Ethics and Regulatory Barriers to Research in Emergency Settings;Annals of Emergency Medicine;2018-10

5. Approaches to community consultation in exception from informed consent: Analysis of scope, efficiency, and cost at two centers;Resuscitation;2018-09

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