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1Notification 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)
2Notification of the Ministry of Public Health Re: Rules, Procedures and Conditions for Modern Drug Distribution, B.E. 2564 (2021)*
3Notification of the Food and Drug Administration Re: Guidelines for the Consideration of Low-Risk Medicinal Product Registrations
4Ministerial Regulation on Renewal of Drug Formula Registration Certificates, B.E. 2566 (2023)*
5Notification of the Food and Drug Administration Re: Guidelines for the Consideration of Applications for Modern Drug Registrations Submitted through Electronic Means (No.2)
6Notification of the Food and Drug Administration Re: Guidelines for the Consideration of Applications for Modern Drug Registrations Submitted through Electronic Means
7Notification of the Ministry of Public Health Re: Rules, Procedures and Conditions for Herbal Product Importation and Sale, B.E. 2566 (2023)*
8Notification of the Ministry of Public Health Re: Type 1, Type 2, Type 4, and Type 5 Narcotic Transit Inspection, B.E. 2567 (2024)*
9Ministerial Regulation No. 24 (B.E. 2537 (1994)) Issued under the Drugs Act, B.E. 2510 (1967)*
10Notification of the Food and Drug Administration Re: Prescribing the Psychotropic Substance Inspection Form in The Case of Import, Export or Transit
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สำนักงานคณะกรรมการอาหารและยา

FOOD AND DRUG ADMINISTRATION

Food and Drug Administration, Ministry of Public Health
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