IRB practices and policies regarding the secondary research use of biospecimens-Reference-Cited by-同舟云学术

IRB practices and policies regarding the secondary research use of biospecimens

Published:2015-05-08 Issue:1 Volume:16 Page:
ISSN:1472-6939
Container-title:BMC Medical Ethics
language:en
Short-container-title:BMC Med Ethics

Author:

Goldenberg Aaron J,Maschke Karen J,Joffe Steven,Botkin Jeffrey R,Rothwell Erin,Murray Thomas H,Anderson Rebecca,Deming Nicole,Rosenthal Beth F,Rivera Suzanne M

Publisher

Springer Science and Business Media LLC

Subject

Health Policy,Health (social science),Issues, ethics and legal aspects

Link

http://link.springer.com/article/10.1186/s12910-015-0020-1/fulltext.html

Reference21 articles.

1. Rothstein MA. The role of IRBs in research involving commercial Biobanks. J Law Med Ethics. 2002;30(1):105–8.

2. Haga SB, Beskow LM. Ethical, legal, and social implications of biobanks for genetics research. Adv Genet. 2008;60:505–44.

3. Winickoff DE, Winickoff RN. The Charitable Trust as a Model for Genomic Biobanks. N Engl J Med. 2003;349(12):1180–4. Print.

4. Wolf LE, Catania JA, Dolcini MM, Pollack LM, Lo B. IRB chairs’ perspectives on genomics research involving stored biological materials: ethical concerns and proposed solutions. J Empir Res Hum Res Ethics. 2008;3(4):99–111.

5. Edwards T, Cadigan J, Evans JP, Henderson G. Biobanks containing clinical specimens: defining characteristics, policies, and practices. Clin Biochem. 2013;47(4-5):245–51.

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