| Literature DB >> 15570740 |
Abstract
Informed consent in clinical research is a matter of both ethics and federal regulation. A research subject must enter a study voluntarily, be informed about risks and benefits, and understand the difference between experiment and treatment.Mesh：
Year: 2004 PMID： 15570740 DOI： 10.3949/ccjm.71.11.907
Source DB: PubMed Journal: Cleve Clin J Med ISSN： 0891-1150 Impact factor: 2.321