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Pesticide Registration

From dossier pre-review to certificate in hand — fully managed, predictable timeline, trackable progress.

Coverage

All Product Categories Under DOA, DLD & FDA

From conventional chemicals to biopesticides, we know the submission pathway. Registration types cover technical-grade, formulated products, label variation and renewal.

Herbicides

Glufosinate, glyphosate and other mainstream AIs

Fungicides

Triazoles, strobilurins and more

Insecticides

Neonicotinoids, pyrethroids and more

Plant Growth Regulators

Plus biopesticides and adjuvants

What We Actually Do

  • Product classification & pathway assessment, including banned/restricted screening
  • Dossier completeness pre-review and format normalisation
  • Field trial design, execution and data collection
  • Dossier compilation, translation and submission to DOA / DLD / FDA
  • Official query responses and technical defence support
  • Post-approval renewal, variation and annual maintenance
Kick-off Checklist

What to Prepare Before We Start

The more complete the dossier, the more accurate the pre-review and the lower the rejection risk. We can also help fill gaps.

  • Active ingredient details (CAS no., purity, source)
  • Formulation and product type
  • Toxicology, residue and environmental data (or existing reports)
  • Home-country registration / Certificate of Free Sale
  • Proposed label and packaging artwork
  • Power of Attorney (if we file on your behalf)

FAQ

How long does a full registration take?
Conventional chemical pesticides typically take 12–24 months including field trials. Biopesticide pathways can be shorter; new AIs or incomplete dossiers take longer. We give a product-specific estimate at the assessment stage.
Can I register without a Thai entity?
You generally need a legal Thai entity as the certificate holder. If you don’t have one, we can set it up first — that’s exactly why our service is end-to-end.
What does it cost?
It depends on product category, whether field trials are needed, and dossier completeness. After assessment we give a clear range covering both official fees and our service fee — no hidden items.
Can you take over a rejected submission?
Yes. We first diagnose the rejection cause — dossier defect, format issue or policy restriction — then propose a remedy and a resubmission timeline.
What happens after approval?
Renewals, formulation or label variations, annual filings, and alignment with import and storage permits. We provide annual maintenance so your certificate never lapses.

Need a Plan Tailored to Your Product?

Tell us your active ingredient, formulation and target market. We’ll come back with feasibility and a cost range within 1–2 weeks.

Get Free Assessment