Mandatory standards
Products within a compulsory standard’s scope require the applicable manufacturing or import authorisation. Check the specifications and effective date before committing to production or shipping.
UnionSPACE coordinates product assessment, factory audit preparation, laboratory testing and TISI licence applications. Start with your product details and we will map the appropriate route.
Private advisory and application support. UnionSPACE is independent of TISI; licensing decisions remain with the authority.
The first question is whether a mandatory Thai industrial standard covers your product and proposed activity.
Products within a compulsory standard’s scope require the applicable manufacturing or import authorisation. Check the specifications and effective date before committing to production or shipping.
A product outside a mandatory scope does not automatically need the same import licence. Voluntary certification and other product requirements should be considered separately.
The responsibilities of a manufacturer, importer and reseller are different.
Assess the licensing requirements before starting production of goods subject to a mandatory standard. Voluntary marking has a separate application basis.
Confirm the importing entity and the product, factory and model coverage. Another importer’s licence is not automatically available for your company to use.
Check the source, compliance records and required marking of the goods you sell. If you also import, review the importer obligations separately.
Testing samples, non-sale use and re-export require a route-specific review. Confirm any permission or notification before dispatch.
These examples are an assessment starting point, not a definitive list of controlled products. Scope depends on the model, specifications and applicable standard.
Rice cookers, fans, refrigerators, air conditioners, irons and hair dryers. The relevant model and standard scope must be checked.
Power strips, power banks, cables and related electrical accessories. Review the technical specifications before ordering.
Motorcycle helmets, tyres, vehicle safety glass and seat belts. Product design and intended use affect the assessment.
Structural steel and other construction materials. Match the product’s grade, dimensions and use to the applicable requirements.
Check both the current scope and effective date when planning a future shipment or product launch.
Send the product name, photos and specification sheet. We will assess the applicable route before recommending application work.
Marketplace document checks can affect your launch as well as Customs clearance.
Before advertising or listing controlled products, confirm the importer or manufacturer, required approvals, product marking and the records your platform requests. If you import the goods yourself, assess your own authorisation requirements.
We review your planned sales channel alongside the product file so the application and launch plan use the same product and applicant details.
We organise the agreed work around your product, factory and applicant. The detailed sequence and evidence depend on the applicable route.
Review the product’s specifications, intended use, model range and applicable standard. Confirm whether mandatory licensing or another route applies.
Coordinate company and factory documentation and the relevant e-License registration steps, including overseas manufacturing information.
Prepare the quality-control file and liaise with the factory and the relevant inspection body on the agreed assessment requirements.
Confirm samples and the laboratory route accepted for the application. Coordinate submission, progress tracking and responses to findings.
Compile the application and supporting reports, coordinate responses and explain the approved scope and marking requirements following a successful decision.
Start with the information you have. We will confirm the detailed checklist once the product and route are assessed.
| Company information | Thai company affidavit and applicant details; signing authority and authorisation documents as applicable. |
|---|---|
| Product identity | Product name, brand, model list, photographs and detailed technical specifications. |
| Manuals and drawings | Instructions, technical drawings and supporting design information relevant to the product. |
| Factory information | Manufacturer name, production address, registration details and available quality-system records. |
| Existing assessment records | Any TISI factory registration, conformity documents, laboratory reports and certificates already available. |
| Shipment and label information | Commercial invoice or planned shipment details, proposed label artwork and intended launch date. |
Licensing is the beginning of ongoing product compliance. We can explain the next steps within your agreed service scope.
Confirm the applicable TIS mark, standard number, traceability and QR-code requirements for the product and approval.
A new factory, design, material or product model may require further assessment or a change to the approved scope.
Keep relevant product, supplier, quality-control and import records available for follow-up requirements.
Explain the approved products, marking and documentation to retailers, distributors and online sales teams.
Connect the factory, importing company and application work through one team.
English, Thai, Chinese and Russian communication helps connect your company, factory and application team.
Product review, factory preparation, testing coordination and application support are organised through an agreed engagement.
We start by assessing what applies, including whether a mandatory application is appropriate for the proposed activity.
Discuss company setup, import coordination and any separate FDA or NBTC assessment with the same team.
There is no single price or timeline that fits every TISI application.
We set out the agreed assessment, documentation, factory liaison, testing coordination and application support, including the responsibilities of your company and manufacturer.
The quotation identifies professional fees and any official fees, laboratory charges, inspection costs, samples, travel, translations or other third-party expenses included or excluded.
Direct answers before preparing your application.
A supplier’s factory assessment or a licence held by a different importer does not automatically authorise your company’s imports. For mandatory-standard imports for sale, the licence is issued to the importer. We review the applicant, factory, product and existing records before confirming the application route.
TISI is the Thai Industrial Standards Institute under the Ministry of Industry. It administers Thai industrial standards and licensing. Whether a licence is required depends on the product, the applicable standard and the proposed manufacturing or import activity.
No. Mandatory requirements apply to products within the scope of compulsory standards. We assess the specifications and intended use against the relevant scope and effective date, rather than relying on a general product category alone.
A retailer reselling goods is in a different position from a business that imports or manufactures them. If you are also the importer, your own import authorisation may be required. Sellers should verify the goods’ compliance, marking and traceability and check the documentation requested by their marketplace.
Yes. The import application process includes assessment of the manufacturing factory, including overseas factories. The applicable requirements and any existing TISI factory registration or accepted conformity records must be checked for the specific application.
Do not assume so. Acceptance depends on the specific standard and TISI’s requirements. Send the certificates and reports you hold so we can assess their relevance and identify any further testing or factory assessment needed.
Timing and costs depend on the standard, product models, technical file, factory readiness, inspection arrangements, laboratory availability and any corrective work. We provide a case-specific scope and indicative schedule after reviewing your product and factory details. Approval is determined by TISI.
Special-purpose imports can follow different requirements. Their eligibility, documentation and any notification or permission should be confirmed before shipment. A non-sale or re-export purpose does not by itself establish an exemption.
Some products need a separate regulatory review in addition to TISI. We can coordinate a wider assessment based on the product’s function, claims and intended use, including whether FDA or NBTC requirements should be investigated.
We can discuss Thai company setup or assess whether an agreed Importer of Record arrangement is suitable. The importer, licence holder, product coverage and commercial responsibilities must be established before accepting the project. An importer arrangement does not remove product approval requirements.
Send the product name, photos, specifications and factory location. Tell us who will import it and your target launch date. We will assess the route and explain the next steps.
Our team speaks English, Chinese (Mandarin), Russian, Kazakh, Burmese, Thai, and Indonesian — Monday to Friday, 9AM–6PM Bangkok time.
Leave us a message and a UnionSPACE representative will contact you within 12 hours.
UnionSPACE is a private service provider and is not affiliated with TISI or any government authority. You may apply directly through the relevant official channels. Professional fees are separate from official and third-party charges unless expressly included. Product coverage, approval and timing depend on the applicable requirements and the authority’s decision.