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    • Postmarket Requirements and Commitments

    Metadata Updated: July 11, 2025

    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 July 11, 2025

    Metadata Source

    Harvested from Healthdata.gov

    Other Data Resources

    Additional Metadata

    Resource Type Dataset
    Metadata Created Date November 10, 2020
    Metadata Updated Date July 11, 2025
    Publisher U.S. Food and Drug Administration
    Maintainer
    Identifier bf085673-ae08-4807-8ca7-aeb36dde83ed
    Data First Published 2021-02-25
    Data Last Modified 2011-02-10
    Category FDA
    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 57ebae47-7df0-42e2-8d0f-b11925a2bdd6
    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 613a9ac981d72e8cc72a165503ef8de6155bb823580d40777ac23748fac4e00f
    Source Schema Version 1.1

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