Six stages — what each delivers, what we do, and what you need to provide. All laid out.
Product classification, dossier pre-review, feasibility check
Dossier compilation & submission to DOA / DLD / FDA
Official lab tests & local trials
Final dossier review & query responses
Official approval & issuance
Variations & certificate renewal
Determine product category, the applicable registration pathway and any banned/restricted risk, then pre-review your existing dossier for completeness. Deliverables: feasibility report, dossier gap list, timeline and cost estimate. You provide: AI details, formulation, existing test data.
We collate and translate the documents into Thai, compile the dossier, submit formally to DOA / DLD / FDA, then track acceptance and answer official queries. Deliverables: submission receipt and acceptance number. You provide: power of attorney, certificate-of-origin documents and product technical data.
The official laboratory tests sample composition and content, while we design and run local field trials in parallel — collecting efficacy and residue data and compiling the reports. Deliverables: official test reports, trial protocols, efficacy and residue reports. You provide: sufficient original-packaged samples, trial samples and technical support. Note: crop seasons directly affect timing and must be scheduled ahead; test results that don't match the dossier are the most common cause of rejection and resubmission.
Consolidate test and trial reports into the final dossier for official review, track progress end-to-end and respond to queries promptly. Deliverables: final dossier, query responses. Note: queries carry response deadlines — delays push the review back or trigger rejection.
Complete the approval process and obtain the pesticide registration certificate, then plan your product launch. Deliverables: pesticide registration certificate. Our role: track progress end-to-end and follow up proactively.
Label filing, packaging updates, information change filings, and renewal after the 6-year validity period. Deliverables: annual compliance calendar, variation filings, certificate renewal.
Delays rarely come from the authority — they come from inadequate preparation. These four are the main culprits.
The most common cause. One missing test report can trigger a full rejection round — months lost.
Field trials are bound by planting cycles — miss a season and you wait a year.
Without a compliant Thai entity, or if business scope excludes pesticides, filing gets blocked.
Official queries carry response deadlines; missing data means deferral.
Tell us your active ingredient, formulation and target market. We’ll come back with feasibility and a cost range within 1–2 weeks.