Clinical Trials Registration and Results Submission

The Department of Health and Human Services proposed requirements for submitting registration and summary results information, including adverse event information, for specified clinical trials of drugs and devices to ClinicalTrials.gov

Action
Published Date
Code CFR
42 C.F.R. Part 11
Contact Information
Jerry Moore, 301-496-4607
More Information
http://www.gpo.gov/fdsys/pkg/FR-2014-11-21/pdf/2014-26197.pdf
Pages
69565-69680
Program Area
Volume Number
79