Home > FAQs > ClinicalTrials.gov - What is the FDAMA? |
The Food and Drug Administration Modernization Act (FDAMA) was passed by the U.S. Congress in 1997 and contains a number of sections related to the regulation of food, drugs, devices, and biological products.
In particular, Section 113 - Information Program on Clinical Trials for Serious and Life-Threatening Diseases, "requires the U.S. Department of Health and Human Services, through the National Institutes of Health, to establish a registry of clinical trials for both federally and privately funded trials of experimental treatments for serious or life-threatening diseases."
Return to the top | Return to the list of FAQs
http://www.nlm.nih.gov/services/ctfdama.html
Last reviewed: 11 October 2006
Last updated: 11 October 2006
First published: 01 January 2001
Metadata| Permanence level: Permanence Not Guaranteed