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Compliance & quality

Compliance & Quality

How a program is controlled before it ships: producing-site qualification, destination-market entry for the European Union and the United States, the documents that travel with each lot, and the controls behind them.

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A clearer way to work

One qualification standard for every producing site, whatever the destination.

Every producing site is qualified before it enters a program: HACCP as the baseline, a recognised food-safety certification - FSSC 22000, BRCGS, IFS Food, or ISO 22000 where a buyer accepts it - with the certificate, its scope and its expiry confirmed in writing for the selected product, and the registrations the destination market requires. What is verified, and what ships with each lot, is set out below.

Food product packaging and documentation coordination for international sourcing

Control points

Verified before the first order, repeated on every lot.

Qualification happens once per producing site and product; release happens on every lot, against the same agreed specification.

  • Certificate, scope and expiry confirmed for the product
  • Destination requirements checked before quotation
  • Batch analysis and documents reviewed before the goods move

What is verified

The checks behind every program.

Producing-site qualification

The site is audited before it enters a program. Current food-safety certification is mandatory, and the certificate, its scope and its expiry are confirmed in writing for the specific product. Sites shipping to the United States must also hold a current FDA food facility registration.

European Union entry

Products for the European Union are checked against the food-law framework for the product and origin concerned: labelling to Regulation (EU) No 1169/2011, contaminant maximum levels under Regulation (EU) 2023/915, pesticide residue limits under Regulation (EC) No 396/2005, and the reinforced official import controls of Regulation (EU) 2019/1793 where they apply. Where a product is subject to border control, the pre-notification is arranged before arrival.

United States entry

FSVP, FDA food facility registration, Prior Notice and, for low-acid and acidified foods, FCE and SID registration of the plant and the process. Set out on the US import compliance page.

Documents per shipment

Each shipment carries the commercial invoice, packing list and transport document, the certificate of origin - with preferential-origin documentation where the destination allows it - a batch-specific certificate of analysis against the agreed specification, and the health, phytosanitary or fumigation certificates the product and destination require.

Controls, traceability and withdrawal

Certified producing sites maintain lot traceability from raw-material reception through processing to dispatch, a documented withdrawal and recall procedure, and complaint and non-conformance handling with corrective action. ALPHATRADE confirms these procedures for the selected site before the first order and carries any buyer complaint through to closure.

Audits, attestations and inspection

Buyer or third-party audits of the producing site are arranged as part of program qualification. Ethical audit reports (SMETA or BSCI) and Halal certification are available from selected producing sites and confirmed for the program before order; organic certification is available for the herbs and botanicals range on request. Independent pre-shipment inspection (SGS or equivalent) is arranged on request at loading.

The working process

01

Site qualification

The producing site is audited and its certification, scope and expiry confirmed for the specific product.

02

Destination review

Labelling, contaminant and residue requirements, registrations and controls are checked for the product and the destination before the program is quoted.

03

Release and shipment

Lot analysis, certificates and shipping documents are assembled and reviewed against the destination requirements before the goods move.

Common questions

Start with the details that matter.

Do you supply the European Union and the United States under the same standard?

Yes. The producing-site qualification is the same for every destination. What differs is the destination review: EU labelling, contaminant and residue rules on one side; FSVP, FDA registration, Prior Notice and, where applicable, FCE and SID on the other. Both are checked before the program is quoted.

Can we audit the producing site?

Yes. Buyer or third-party audits are arranged as part of program qualification, and certification documents, scope and expiry for the selected site are provided to qualified buyers before the first order.

Which additional attestations are available?

Ethical audit reports (SMETA or BSCI) and Halal certification are available from selected producing sites and confirmed for the program before order. Organic certification is available for the herbs and botanicals range on request.

What happens if a lot does not meet the specification?

A lot that fails release against the agreed specification is not shipped; it is corrected or replaced before the goods move. A non-conformance found after delivery is recorded, investigated with the producing site and closed with corrective action, and the outcome is carried into subsequent orders.

Do you arrange independent inspection?

Yes. Independent pre-shipment inspection (SGS or equivalent) is arranged on request at loading, and the inspection report travels with the shipping documents.

Which documents accompany a shipment to the European Union?

Commercial invoice, packing list and transport document; certificate of origin, with EUR.1 or an origin declaration where preferential origin applies; a batch certificate of analysis; and the health, phytosanitary or fumigation certificates required for the product. The exact set is fixed on the program specification.

Professional buyer enquiries

Send the requirement. We will review the commercial fit.

Your requirement does not need to be complete. Share what you know: product, quantity, destination, packaging requirements and timing. ALPHATRADE will review the scope and outline the next commercial step.

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