Medicines and herbal products registration
Imported modern medicines are registered under the Drug Act B.E. 2510; products with herbs as key ingredients fall under the Herbal Products Act B.E. 2562, with three routes by risk: notification, detailed notification or full registration. Every key step of our drug and herbal work is reviewed and signed off by a pharmacist.
How the work runs
The five stages, end to end
- 1
Classification and route
Handled by: Company + pharmacist · Time: 1–2 weeks
Drug or herbal product; for herbal products, notification, detailed notification or registration depending on complexity and how serious the indication is.
- 2
Premises licence
Handled by: Thai FDA · Time: About 1–2 months
Licence to import medicines (with a responsible pharmacist and storage) or herbal products.
- 3
Dossier and GMP
Handled by: Manufacturer + company · Time: 1–3 months
Herbal formula and evidence of use; for medicines, the foreign manufacturer's GMP clearance and an ASEAN CTD dossier.
- 4
Pharmacist review and filing
Handled by: Pharmacist + Thai FDA · Time: Set by Thai FDA
A pharmacist signs off the dossier before submission; Thai FDA review time depends on the route.
Costs
| Item | Amount | Source |
|---|---|---|
| Thai FDA consideration fees | By route (MOPH fee notifications) | Official rate |
| Registration service with pharmacist review | Quoted per product and route | PUNNAKA quotation |