Exporting to the US

US FDA Compliance

Your Partner for US Food Export Compliance

We offer comprehensive support for food exporters targeting the US market. From FDA filings and facility registration to assisting with import detention issues, inspection reports and third party audits, we’re your one-stop shop for compliance.

Proactive Compliance & Issue Resolution for US Exports

We help you proactively maintain compliance with US-FDA regulations through third-party audits and process deviation evaluations. Should issues arise, we provide expert support with import detentions, alerts, and inspection reports, ensuring that your products regain proper FDA compliance, to get you back in business.

US FDA filing and facility registration

Filing products with the FDA for export to the US involves much more than filling out forms. Technical compliance of your aseptic processing and packaging system must be demonstrated throughout a third-party audit. Our professionals have 30+ years of experience in the field. Let us help you making the journey throughout US exports a smooth one!

US FDA import detention and import alerts

We offer assistance when FDA issues a notice of detention that stops the product from entering the US. Detentions happen whenever a product seems to violate FDA regulations. Product detentions are costly and could damage the company reputation if not handled fast and properly. When FDA issues an import alert, the product is automatically detained. To be removed from an import alert, the processor must send to FDA proof that the product complies with FDA regulations. This process can be long and costly.

Deviation handling

Process deviations often occur in every processing plant. Appropriate handling of the product and disposition determination can be a real headache. Let us help you with that! By reviewing the processing deviation documentation, making calculations, and occasionally performing further testing, we can determine the appropriate product disposition. We also write process deviation letters, which are mandatory for any product for the US market that undergoes a process deviation.