Encouraging translational research through harmonization of FDA and Common Rule informed consent requirements for research with banked specimens

Journal of Legal Medicine

Volumn 27, Issue 2, 2006, Pages 119-166

  Evans, Barbara J ^a,b,e   Meslin, Eric M ^a,c,d,f  

^a Indiana University   (United States)

^b INDIANA UNIVERSITY   (United States)

^c INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d School of Liberal Arts   (United States)

^e School of Liberal Arts ^*  (United States)

^f ELI LILLY AND COMPANY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOTECHNOLOGY; FOOD AND DRUG ADMINISTRATION; HEALTH CARE FACILITY; HEALTH CARE PLANNING; HEALTH CARE POLICY; HUMAN; INFORMED CONSENT; LAW; MEDICAL ETHICS; MEDICAL RESEARCH; PRIVACY; REVIEW; RISK ASSESSMENT; STANDARD; UNITED STATES; ARTICLE; COMMERCIAL PHENOMENA; CONFIDENTIALITY; ETHICS; GOVERNMENT REGULATION; HEALTH INSURANCE; HUMAN EXPERIMENT; LABORATORY DIAGNOSIS; LEGAL ASPECT; METHODOLOGY; POLICY; PRACTICE GUIDELINE;

BIOLOGICAL SPECIMEN BANKS; BIOMEDICAL RESEARCH; COMMERCE; CONFIDENTIALITY; GOVERNMENT REGULATION; GUIDELINES; HEALTH INSURANCE PORTABILITY AND ACCOUNTABILITY ACT; HUMAN EXPERIMENTATION; HUMANS; INFORMED CONSENT; PUBLIC POLICY; SPECIMEN HANDLING; UNITED STATES; UNITED STATES FOOD AND DRUG ADMINISTRATION;

EID: 33745956333     PISSN: 01947648     EISSN: 1521057X     Source Type: Journal    
DOI: 10.1080/01947640600716366     Document Type: Review

References (0)