Encouraging translational research through harmonization of FDA and common rule informed consent requirements for research with banked specimens

J Leg Med. 2006 Jun;27(2):119-66. doi: 10.1080/01947640600716366.

Authors

Barbara J Evans¹, Eric M Meslin

Affiliation

¹ Program in Pharmacogenomics, Ethics, and Public Policy, Indiana University Center for Bioethics, Indianapolis 46202, USA. bjevans@iupui.edu

PMID: 16728351
DOI: 10.1080/01947640600716366

No abstract available

Publication types

Legal Case
Research Support, Non-U.S. Gov't

MeSH terms

Biological Specimen Banks / legislation & jurisprudence*
Biomedical Research / ethics
Biomedical Research / legislation & jurisprudence*
Commerce / legislation & jurisprudence
Confidentiality / legislation & jurisprudence*
Government Regulation
Guidelines as Topic*
Health Insurance Portability and Accountability Act
Human Experimentation / ethics
Human Experimentation / legislation & jurisprudence
Humans
Informed Consent / legislation & jurisprudence*
Public Policy*
Specimen Handling / ethics
Specimen Handling / methods
United States
United States Food and Drug Administration*