Build the U.S. project file before the first order.

This export intake collects the business facts needed to open three controlled workstreams: facility registration readiness, product/SKU review, and importer–broker alignment.

Start the launch kit Review current documents

Three controlled workstreams

Do not let a quotation outrun the documentation.

These steps organize commercial preparation. They do not confirm FDA registration, ingredient acceptability, label approval, FSVP compliance or an APHIS permit.

Facility readiness

Confirm the legal entity, physical production site, FDA registration status, U.S. agent and UFI/DUNS information for the exact facility involved.

Three-SKU review

Place the first three candidate SKUs under an ingredient, intended-use, label and claim review before sales materials or artwork are released.

Importer & broker route

Identify the importer-of-record, FSVP owner, target states, customs broker and any animal-origin/APHIS screen required.

U.S. Export Launch Kit

A practical project file—not a generic enquiry.

Send the information you have. Blank fields are acceptable where facts are not yet known; the export team will mark what needs confirmation.

Facility and U.S. agent factsFirst three candidate SKUsIntended use, key ingredients and draft claimsImporter-of-record and FSVP ownershipTarget states and customs broker

Send documentation by email

01Facility registration readinessCollect facts only. Do not enter registration numbers unless independently confirmed.

Legal entity / facility name *

Physical production site *

FDA facility registration status

U.S. agent / UFI-DUNS status

02Three-SKU ingredient, claim and label screenState the intended use plainly; avoid disease treatment, prevention or mitigation claims.

SKU 1: format, species, intended use, key ingredients and draft claims *

SKU 2: format, species, intended use, key ingredients and draft claims

SKU 3: format, species, intended use, key ingredients and draft claims

03U.S. importer and broker alignmentThe U.S. owner/consignee or qualified representative must confirm the relevant FSVP responsibility.

Importer of record / FSVP owner

Customs broker

Target state(s)

Animal-origin ingredient screen

Commercial brief

Send by Email

Important: This intake supports commercial project preparation only. Product classification, ingredients, claims, labels, FDA registration, U.S. agent/UFI, FSVP ownership, state requirements, APHIS permits and entry documentation must be verified for each SKU by the applicable responsible parties.