Skip to main content

The Development and Operation of IRBs: Medical Regulations and Social Science

Buy Article:

$53.17 plus tax (Refund Policy)

Abstract:

A sketch of the development of institutional review boards (IRBs) and the system of human subjects research regulation in the United States is presented, from the Nuremberg Code of 1949 to the Belmont Report of 1979, and continues with several contemporary developments. Conflicts within the system are discussed, particularly those related to the regulatory application of the medical model to social science. Examination of two central documents produced by participants in the IRB regulatory system is presented to illustrate difficulties with current regulation.

Keywords: Human Subjects Research; Institutional Review Board

Document Type: Research Article

DOI: http://dx.doi.org/10.1080/00909880500149353

Affiliations: Mass Communication, American University of Sharjah, United Arab Emirates

Publication date: August 1, 2005

Access Key

Free Content
Free content
New Content
New content
Open Access Content
Open access content
Partial Open Access Content
Partial Open access content
Subscribed Content
Subscribed content
Free Trial Content
Free trial content
Cookie Policy
X
Cookie Policy
Ingenta Connect website makes use of cookies so as to keep track of data that you have filled in. I am Happy with this Find out more