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Postmarket Requirements and Commitments

Metadata Updated: August 2, 2021

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.

Access & Use Information

Public: This dataset is intended for public access and use. License: See this page for license information.

Downloads & Resources

Dates

Metadata Created Date November 10, 2020
Metadata Updated Date August 2, 2021

Metadata Source

Harvested from Healthdata.gov

Additional Metadata

Resource Type Dataset
Metadata Created Date November 10, 2020
Metadata Updated Date August 2, 2021
Publisher U.S. Food and Drug Administration
Unique Identifier Unknown
Maintainer
Identifier bf085673-ae08-4807-8ca7-aeb36dde83ed
Data First Published 2021-02-25
Data Last Modified 2011-02-10
Public Access Level public
Bureau Code 009:10
Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
Metadata Catalog ID https://healthdata.gov/data.json
Schema Version https://project-open-data.cio.gov/v1.1/schema
Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
Harvest Object Id 1b172cb5-7aef-476d-bf83-b299cc89116f
Harvest Source Id 651e43b2-321c-4e4c-b86a-835cfc342cb0
Harvest Source Title Healthdata.gov
Homepage URL http://www.fda.gov/Drugs/InformationOnDrugs/ucm142931.htm
License http://opendefinition.org/licenses/odc-odbl/
Program Code 009:002
Source Datajson Identifier True
Source Hash 33f40985712e1e349607e98558c5dec82c38d651
Source Schema Version 1.1

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