Facility readiness review
Identify key facility details, responsible contacts and information gaps before starting the process.
Independent compliance assistance service. Gloway is not the U.S. FDA.
We help eligible food facilities organize the information and coordination needed for registration. Requirements depend on the facility, activities and products.
Identify key facility details, responsible contacts and information gaps before starting the process.
Support preparation and submission coordination through the official FDA process, including U.S. agent arrangements where applicable.
Help organize confirmation records and track the FDA's biennial registration renewal cycle.
Tell us about your business and facility.
We identify the information and support required.
Review assistance fees and U.S. agent arrangements, if needed.
Proceed through the FDA registration process.
Keep records and plan for renewals or updates.
Share your initial business information. A Gloway team member can then advise on the next steps and service scope.
Explore how registration assistance requests will move through review, payment coordination, filing assistance and renewal tracking. This dashboard uses illustrative sample data; it is not connected to real customer records.
See the current stage, information requested by the team, and the next milestone.
Assign an owner, review information, and document the next step for each request.
Track biennial renewal windows and facility information changes once securely implemented.
Select a workflow stage to preview what the manufacturer and Gloway operations team would see. No changes are saved.
No. Food facility registration is not FDA approval, certification, or an endorsement of a facility or its products.
The FDA does not charge a fee to register a food facility. Gloway may charge separately for assistance, coordination and related services.
No. Applicability depends on the facility's activities and exemptions. We assess the circumstances before recommending a process.
Registrations subject to the requirement must generally be renewed every even-numbered year between October 1 and December 31.
No. FDA processes and import admissibility depend on applicable requirements and official decisions. Registration alone does not guarantee that a shipment will be admitted.