Provides information to the public on postmarket requirements and commitments. The phrase postmarket requirements and commitments refers to studies and clinical trials that sponsors conduct after approval to gather additional information about a product's safety, efficacy, or optimal use. Some of the studies and clinical trials may be required; others may be studies or clinical trials a sponsor has committed to conduct.
Data and Resources
Dept. of Health & Human Services
Center for Drug Evaluation and Research
U.S. Food and Drug Administration > Center for Drug Evaluation and Research
|Program Code|| |
009:002 - Department of Health and Human Services - Human Drugs