QFA - Qualified Facility Attestation Submission

Required documents vary by product category but typically include: company registration details, product specifications, manufacturing facility information, and authorized representative documentation. Our team provides a complete checklist based on your specific needs.

Staying compliant is a continuous, year-round obligation. Our team proactively manages all mandatory filings to avoid costly penalties or loss of good standing. We manage and file all required annual reports in every state your company is registered in, ensuring you never miss a deadline. We conduct thorough reviews of your company's status in all relevant jurisdictions to identify and rectify any compliance gaps before they become a problem.

FDA registrations require periodic renewal depending on product category (annual or bi-annual). TABS manages all renewals proactively, ensuring you never miss a deadline and remain compliant.

Yes, TABS serves as your official U.S. FDA Agent, acting as your representative for all FDA communications and compliance matters. We have been an official FDA Agent since 2014.

Yes, TABS provides comprehensive label and ingredient review services to ensure full FDA compliance before your products reach U.S. customs.