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Results: 1 to 20 of 1194

1.

Ethical problems in health research with indigenous or originary peoples in Peru.

Minaya G, Roque J.

J Community Genet. 2015 Jun 24. [Epub ahead of print]

PMID:
26103916
2.

Research findings with clinical implications.

Bjugn R.

Tidsskr Nor Laegeforen. 2015 May 5;135(8):755-8. doi: 10.4045/tidsskr.14.0861. eCollection 2015 May 5. English, Norwegian.

3.

On the Alleged Right to Participate in High-Risk Research.

Różyńska J.

Bioethics. 2015 Feb 3. doi: 10.1111/bioe.12146. [Epub ahead of print]

PMID:
25644532
5.

The shell game: how institutional review boards shuffle words.

Whitney SN.

J Transl Med. 2014 Aug 14;12:201. doi: 10.1186/1479-5876-12-201.

6.

Variability in IRBs regarding parental acceptance of passive consent.

Higgerson RA, Olsho LE, Christie LM, Rehder K, Doksum T, Gedeit R, Giuliano JS Jr, Brennan B, Wendlandt R, Randolph AG; PALISI PICFlu Study Investigators.

Pediatrics. 2014 Aug;134(2):e496-503. doi: 10.1542/peds.2013-4190. Epub 2014 Jul 7.

PMID:
25002659
7.

Analysis of warning letters issued by the US Food and Drug Administration to clinical investigators, institutional review boards and sponsors: a retrospective study.

Shetty YC, Saiyed AA.

J Med Ethics. 2015 May;41(5):398-403. doi: 10.1136/medethics-2013-101829. Epub 2014 Jun 25.

PMID:
24965716
8.

Child's assent in research: age threshold or personalisation?

Waligora M, Dranseika V, Piasecki J.

BMC Med Ethics. 2014 Jun 13;15:44. doi: 10.1186/1472-6939-15-44.

9.

Using police crash databases for injury prevention research - a comparison of opt-out and opt-in approaches to study recruitment.

Elkington J, Stevenson M, Haworth N, Sharwood L.

Aust N Z J Public Health. 2014 Jun;38(3):286-9. doi: 10.1111/1753-6405.12237.

PMID:
24890488
10.

A mixed-methods study on perceptions towards use of Rapid Ethical Assessment to improve informed consent processes for health research in a low-income setting.

Addissie A, Davey G, Newport MJ, Addissie T, MacGregor H, Feleke Y, Farsides B.

BMC Med Ethics. 2014 May 2;15:35. doi: 10.1186/1472-6939-15-35.

11.

[Update of the work of the ethics research in evaluating genetic research and its role as an external ethics committee biobank].

Alfonso Farnós I, Hernández Gil A, Rodríguez Velasco M.

Rev Derecho Genoma Hum. 2013 Jul-Dec;(39):173-203. Spanish.

PMID:
24868962
12.

Human subjects protection: an event monitoring committee for research studies of girls from breast cancer families.

Harris D, Patrick-Miller L, Schwartz L, Lantos J, Daugherty C, Daly M, Andrulis IL, Buys SS, Chung WK, Frost CJ, John EM, Keegan TH, Knight JA, Terry MB, Bradbury AR.

J Adolesc Health. 2014 Sep;55(3):352-7. doi: 10.1016/j.jadohealth.2014.03.007. Epub 2014 May 17.

PMID:
24845866
13.

Ethics and regulatory complexities for pragmatic clinical trials.

Sugarman J, Califf RM.

JAMA. 2014 Jun 18;311(23):2381-2. doi: 10.1001/jama.2014.4164. No abstract available.

PMID:
24810723
14.

Is there an ethical obligation to disclose controversial risk? A question from the ACCORD Trial.

DeMarco JP, Ford PJ, Patton DJ, Stewart DO.

Am J Bioeth. 2014;14(4):4-10. doi: 10.1080/15265161.2014.889240.

PMID:
24730479
15.

Federal human research oversight of clinical trials in the United States.

Zarin DA, Tse T, Menikoff J.

JAMA. 2014 Mar 5;311(9):960-1. doi: 10.1001/jama.2013.284306. No abstract available.

16.

Ethical review of health systems research in low- and middle-income countries: a conceptual exploration.

Hyder AA, Rattani A, Krubiner C, Bachani AM, Tran NT.

Am J Bioeth. 2014;14(2):28-37. doi: 10.1080/15265161.2013.868950.

PMID:
24521334
17.

The fiduciary obligation of the physician-researcher in phase IV trials.

Bernabe RD, van Thiel GJ, Raaijmakers JA, van Delden JJ.

BMC Med Ethics. 2014 Feb 7;15:11. doi: 10.1186/1472-6939-15-11.

18.

Variability in research ethics review of cluster randomized trials: a scenario-based survey in three countries.

Taljaard M, Brehaut JC, Weijer C, Boruch R, Donner A, Eccles MP, McRae AD, Saginur R, Zwarenstein M, Grimshaw JM.

Trials. 2014 Feb 5;15:48. doi: 10.1186/1745-6215-15-48.

19.

"It's my blood": ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants.

Moodley K, Sibanda N, February K, Rossouw T.

BMC Med Ethics. 2014 Jan 22;15:4. doi: 10.1186/1472-6939-15-4.

20.

Health literacy and consent forms: librarians support research on human subjects.

Raimondo PG, Harris RL, Nance M, Brown ED.

J Med Libr Assoc. 2014 Jan;102(1):5-8. doi: 10.3163/1536-5050.102.1.003. No abstract available.

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