FOOD · MEDICAL DEVICES · HERBAL PRODUCTS
Thai FDA permits & product registration
Thai FDA coordination for food, medical devices, herbal products and other relevant categories, from product classification submissions to registration and business-specific permit applications.
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SERVICE SCOPE
What we can coordinate
For brand owners, importers, manufacturers and distributors planning product documentation. Share composition, product format and intended use so the team can assess the scope.
Sales permit applications
Import permits
Manufacturing permits
Product classification submissions
BEFORE YOU BEGIN
Information that helps classify a product faster
Thai FDA work should start from the factual product profile rather than the marketing name so the correct regulatory path can be assessed.
- Formula, ingredients or specification
Used to understand the product's composition and technical characteristics.
- Intended use and method of use
Explain who uses the product, how it is used and its physical form.
- Label, artwork and available claims
Helps separate factual label information from marketing claims that may need further review.
- Manufacturer and country-of-origin information
Include manufacturer details, manufacturing site and any available source documents.
- Business activity you plan to conduct
For example import, manufacture, sale or product registration, so establishment-level licences can also be considered.
B2B HANDOVER
Before you hand over the enquiry.
01
Organize information by product
Separate product names, formulas, uses and manufacturers before registration or permit scope is assessed.
02
Separate marketing from product facts
Share specifications, actual use and available label wording so coordination starts from consistent information.
HOW WE WORK
From product classification to a submission-ready dossier
- 01
Classify from the actual product facts
Review formula, intended use, product form and claims to identify the appropriate starting category.
- 02
Separate establishment licences from product registration
Check whether the importer, manufacturer or seller needs business-level licensing before product work proceeds.
- 03
Prepare dossier and label information
Collect manufacturer documents, formula, specifications, labels and category-specific supporting information.
- 04
Submit and respond to observations
Handle the agreed submission scope and coordinate additional information when corrections or further documents are requested.
BUILT FOR PROCUREMENT
A quotation that separates product and establishment work
One product may involve classification, registration, label review and company licensing, so each scope should be visible before work begins.
Product-level scope
State the number of SKUs, formulas or products requiring classification, registration or label review.
Company and premises scope
Identify import, manufacturing, sales or premises-related licences included in the work.
Third-party costs and pending inputs
Separate official fees, testing, translation and manufacturer information that is still outstanding.
Timelines and approval paths differ by product category
Food, medical devices, herbal products and other categories use different requirements and supporting documents, so each product must be reviewed before the work sequence and scope can be confirmed.
GOOD TO KNOW
Before you get started
Which product categories can you review?
The stated services cover food, medical devices, herbal products and related categories. Provide composition, intended use and product format for an initial scope review.
What if we are unsure about the product category?
Share the product name, composition, available label and intended product claims. We can assess classification submission support rather than relying on the trade name alone.
Is product registration the same request as an import permit?
Please identify the product, premises and activity involved. Our team explains the scope proposed for each item instead of treating every step as one unspecified service.
What should we provide for several formulas or pack sizes?
List the formulas, pack sizes, labels and manufacturers separately and explain the differences. This helps align the document review and estimated workload.
Can approval timing be confirmed at the first enquiry?
We can review a working plan from the information received. Agency review and requests for further information can affect timing, so an initial enquiry does not guarantee an approval date.
What should an overseas manufacturer prepare?
Start with available product information, composition, specifications, labels and a manufacturer contact. This is a discussion checklist, not a universal mandatory document list.
REQUEST FOR QUOTATION
Need a quotation for your company?
Share company information, the service and cargo details. Our team reviews the scope before quoting; incomplete information does not generate an automatic price.
Request a quotationREQUEST A CONSULTATION
Tell us about your shipment.
Share a few details so our team can follow up and review the service and documentation you need.
01
Start with your goods and the support you need.
02Our team reviews the details and follows up through your contact channel.
03Discuss the scope and costs before work begins.
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