Informed consent or acknowledgment of disclosure [1]

Clinical Pharmacology and Therapeutics

Volumn 78, Issue 4, 2005, Pages 439-440

  Reidenberg, Marcus M ^a  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL RESEARCH; FOOD AND DRUG ADMINISTRATION; INFORMED CONSENT; INTERPERSONAL COMMUNICATION; LETTER; MEDICAL ETHICS; MEDICAL SCHOOL; PRESCRIPTION; PRIORITY JOURNAL;

CLINICAL TRIALS; DISCLOSURE; EDUCATIONAL STATUS; HUMAN EXPERIMENTATION; HUMANS; INFORMED CONSENT; RISK ASSESSMENT;

EID: 25844486007     PISSN: 00099236     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clpt.2005.07.008     Document Type: Letter

References (9)

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2. F.G. Miller Ethical issues with research in healthy subjects risk-benefit assessment Clin Pharmacol Ther 74 2003 513 515
3. C.C. Doak, L.G. Doak, J.H. Root Teaching patients with low literacy 2nd ed. 1996 JB Lippincott Philadelphia 3 Chap. 1
4. M.K. Paasche-Orlow, H.A. Taylor, F.L. Brancati Readability standards for informed-consent forms as compared with actual readability N Engl J Med 348 2003 721 726
5. J. Ancker Developing the informed consent form a review of the readability literature and an experiment Am Med Writers Assoc J 19 2004 97 100
6. G.J. Annas Reforming informed consent to genetic research JAMA 286 2001 2326 2328
7. L.C. Epstein, L. Lasagna Obtaining informed consent Arch Intern Med 123 1969 682 688
8. R.J. Levine Ethics and regulation of clinical research 2nd ed. 1986 Urban & Schwarzenberg Baltimore 98 Chap. 5
9. Title 21 - Food and drugs. 21 CFR. 208.20. Available from: URL: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart= 208&showFR=1&subpartNode=21:4.0.1.1.8.2 Accessed Aug 30, 2005.