Online Registration of Food Facilities | FDA
As part of the provisions of the Bioterrorism Act of 2002, food facilities are required to register with FDA. This page contains links with information on how to register a food facility.
Registration and Listing | FDA
Domestic and foreign establishments that manufacture, repack, or re-label drug and biologic products, including vaccines, are required to register with the FDA.
The Ultimate Guide To FDA Registrations | FDA Atty
Feb 4, 2025 · Navigating the complexities of FDA registrations is essential for companies. Here, we will showcase the ultimate guide to the types of FDA registration.
Guide to FDA Registration and Listing for Drug Companies
Nov 4, 2024 · Learn the essential steps and requirements for FDA registration and drug listing for pharmaceutical companies. Ensure compliance and market access with expert guidance from …
Search Registration and Listing | FDA
Releasable establishment registration and listing information under the Freedom of Information Act is available by searching the Establishment Registration and Listing database.
Establishment Registration & Device Listing - Food and Drug Administration
Jan 12, 2026 · Note: Registration of a device establishment, assignment of a registration number, or listing of a medical device does not in any way denote approval of the establishment or its products by...
Registration of Food Facilities and Other Submissions | FDA
Specifically, if FDA determines that food manufactured, processed, packed, received, or held by a registered food facility has a reasonable probability of causing serious adverse health ...
Device Registration and Listing | FDA
Sep 30, 2025 · Registration and listing provides the FDA with the location of medical device establishments and the devices manufactured at those establishments.
U.S. Food and Drug Administration
The FDA is committed to ensuring data transparency by promoting timely registration and reporting of results information to ClinicalTrials.gov.
FDA Industry Systems
Oct 31, 2023 · FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including registrations, listings, and other notifications.