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
Dataset InfoThese fields are compatible with DCAT, an RDF vocabulary designed to facilitate interoperability between data catalogs published on the Web.
009:10 - Food and Drug Administration
009:002 - Department of Health and Human Services - Human Drugs
|Public Access Level|
Dept. of Health & Human Services
Center for Drug Evaluation and Research
U.S. Food and Drug Administration > Center for Drug Evaluation and Research
Project Open Data FieldsThese fields are compatible with Project Open Data, an Open Data policy of the US Federal government.