Social Media and Community Engagement in Trials Using Exception From Informed Consent
Author:
Affiliation:
1. From Washington DC VA Medical Center, Washington, DC.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
https://www.ahajournals.org/doi/pdf/10.1161/CIRCULATIONAHA.113.003575
Reference11 articles.
1. National Archives and Records Administration. Code of Federal Regulations Title 21 Volume 1 21CFR50.24. Revised as of April 1 2012.
2. US Department of Health and Human Services Food and Drug Administration. Guidance for informed institutional review boards clinical investigators and sponsors: exception from informed consent requirements for emergency research. March 2011 Updated April 2013. http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM249673.pdf. Accessed on May 28 2013.
3. Exception from Informed Consent Enrollment in Emergency Medical Research: Attitudes and Awareness
4. Conducting research using the emergency exception from informed consent: the Public Access Defibrillation (PAD) Trial experience
5. Recommendations for Implementation of Community Consultation and Public Disclosure Under the Food and Drug Administration’s “Exception From Informed Consent Requirements for Emergency Research”
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