The common rule, updated

New England Journal of Medicine

Volumn 376, Issue 7, 2017, Pages 613-615

  Menikoff, Jerry ^a   Kaneshiro, Julie ^a   Pritchard, Ivor ^a  

^a U S DEPARTMENT OF HEALTH AND HUMAN SERVICES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD SAMPLING; CLINICAL RESEARCH; ETHICAL DECISION MAKING; GOVERNMENT REGULATION; HEALTH CARE QUALITY; HUMAN RIGHTS; INFORMATION DISSEMINATION; INFORMED CONSENT; MEDICAL ETHICS; PATIENT DECISION MAKING; PATIENT PARTICIPATION; PATIENT SAFETY; PRIVACY; PUBLIC OPINION; REVIEW; ETHICS; HUMAN; LEGISLATION AND JURISPRUDENCE; MEDICAL RESEARCH; PROFESSIONAL STANDARD; RESEARCH SUBJECT; SPECIMEN HANDLING; STANDARDS; UNITED STATES;

BIOMEDICAL RESEARCH; ETHICS COMMITTEES, RESEARCH; ETHICS, CLINICAL; GOVERNMENT REGULATION; HUMANS; INFORMED CONSENT; RESEARCH SUBJECTS; SPECIMEN HANDLING; UNITED STATES;

EID: 85013399186     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMp1700736     Document Type: Review

References (3)

1. Department of Health and Human Services. Human subjects research protections: Enhancing protections for research subjects and reducing burden, delay, and ambiguity for investigators. Fed Regist 2011; 76(143): 44512-31.
2. Department of Health and Human Services. Federal policy for the protection of human subjects. Fed Regist 2015; 80(173): 53933- 4061.
3. National Academies of Sciences, Engineering, and Medicine. Optimizing the nation's investment in academic research: A new regulatory framework for the 21st century. Washington, DC: National Academies Press, 2016 (https://www.nap.edu/read/21824/chapter/1).