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Health Products
Health Products
| No. | Title | Status | Download |
|---|---|---|---|
| 1 | Notification of the Food and Drug Administration Re: Guidelines for the Registration of Modern Drugs for Human Use and Amendments to the Drug Registration through the Reference of Evaluation Results from the Collaborative Registration Procedure (CRP) |  |
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| 2 | Notification of the Ministry of Public Health Re: Rules, Procedures and Conditions for Modern Drug Distribution, B.E. 2564 (2021)* | |
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| 3 | Notification of the Food and Drug Administration Re: Guidelines for the Consideration of Low-Risk Medicinal Product Registrations | |
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| 4 | Ministerial Regulation on Renewal of Drug Formula Registration Certificates, B.E. 2566 (2023)* | |
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| 5 | Notification of the Food and Drug Administration Re: Guidelines for the Consideration of Applications for Modern Drug Registrations Submitted through Electronic Means (No.2) | |
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| 6 | Notification of the Food and Drug Administration Re: Guidelines for the Consideration of Applications for Modern Drug Registrations Submitted through Electronic Means | |
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| 7 | Ministerial Regulation No. 24 (B.E. 2537 (1994)) Issued under the Drugs Act, B.E. 2510 (1967)* | |
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| 8 | Documents or Evidence Indicating That Pharmaceutical Chemicals Are Produced by the Places of Production with Manufacturing Quality Certification | |
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| 9 | Self-Checklist for Document Submission for the Application for Traditional Drug Formula Registration | |
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| 10 | Self-Checklist for Document Submission for the Application for Modern Veterinary Drug Formula Registration | |