FDA Compliance Services
Browse registrations, renewals, label reviews, and expert consultations designed for international exporters seeking fast, compliant U.S. market entry.
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Additional Services
FURLS Account Creation and Link FDA Registration
Create a FURLS account (FDA Unified Registration and Listing System) in the FIS (FDA Industry System) and link to your FDA facility's registration.
Additional Services
FDA FFR - Registration Certificate
TABS can issue a company certificate of FDA registration to confirm that the facility has been successfully registered at the FDA Food Facility Registration for the current period.
Alcohol & Beverages
COLA Waiver
TABS will assist you with the compliance to send your wine samples for soliciting orders or trade shows.
Additional Services
DUNS Assistance
This is an FDA requirement beginning October 1st, 2020. TABS will apply for your DUNS number on your behalf.
Food (Human)
FDA FFR Registration (U.S. Facility)
Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
Food (Human)
Renewal FDA FFR (U.S. Facility)
Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
Food (Human)
QFA - Qualified Facility Attestation Submission
This service is included in the FDA FFR Registration service.
Food (Human)
Prior Notice
The Prior Notice has to be filed 2 days prior to the arrival of your samples to the US. We can assist you with the filing.
Food (Human)
Label Review for Foods, Drinks and Dietary Supplements
Label compliance is an important aspect of doing business in the U.S. If your product does not meet the requirements your product could be deemed mislabeled or misleading.
Food (Human)
Ingredients Review for Foods, Drinks and Dietary Supplements
Food ingredients including color additives are regulated by the FDA. If your product does not meet the requirements your product could be deemed adulterated or misleading.
Food (Animal)
FDA FFR Agent and Registration
Food Facility Registration and Agent Service for foreign companies that are engaged in producing, packing, or holding food for human or animal consumption.
Food (Animal)
FDA FFR Registration (U.S. Facility)
Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
Food (Animal)
Renewal FDA FFR
Food Facility Registration and Agent Service Renewal for foreign companies that are engaged in producing, packing, or holding food for human or animal consumption.
Food (Animal)
Renewal FDA FFR (U.S. Facility)
Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
Food (Animal)
QFA - Qualified Facility Attestation Submission
This service is included in the FDA FFR Registration service.
Food (Animal)
Prior Notice
The Prior Notice has to be filed 2 days prior to the arrival of your samples to the US. We can assist you with the filing.
Consultation
FDA Compliance consultation call
TABS will assist you to understand and comply with FDA compliance requirements as an importer.
Food (Human)
FDA FFR Agent and Registration
Food Facility Registration and Agent Service for foreign companies that are engaged in producing, packing, or holding food for human consumption.
Food (Human)
Renewal FDA FFR 2027-28 > Early Bird Discount
Food Facility Registration and Agent Service Renewal 2027-28 for foreign companies that are engaged in producing, packing, or holding food for human consumption. Early bird discount on purchases before Sept 30.
Food (Human)
Renewal FDA FFR 2027-28
Food Facility Registration Renewal for foreign companies that are engaged in producing, packing, or holding food.
Food (Human)
FSVP Importer for Trade Shows
FSVP importers are required to develop, maintain and follow an FSVP for each food imported unless an exemption applies. TABS can help you to comply.
Food (Human)
Food (Human)
Renewal FDA FFR (U.S. Facility) 2027-28 > Early Bird Discount
Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
Medical Devices
Medical Devices Establishment Registration, Device Listing & U.S. Agent Service - FY2027
Establishments engaged in the manufacturing or other activities of medical devices to be marketed in the US need to register the facility, list the devices and name an agent for communication purposes.
Owners or operators of places of business (also called establishments or facilities) that are involved in the production and distribution of medical devices intended for use in the United States are required to register annually with the FDA. (Title 21 CFR Part 807).
Not sure which service you need?
Our FDA compliance experts can help you determine the right services for your products and market entry strategy.
