MARKETING AUTHORIZATION OF VETERINARY PRODUCTS IN THAILAND

  • Rajkumar Gupta

Abstract

The registration of veterinary drugs in Thailand is much easier than human products. The major requirement is samples and associated technical documents. The documents are checked by FDA under Drug Act BE 2510 (1967). If they are properly provided, the samples are released to Department of Medical Sciences for verifying the quality. Once the samples pass the required tests, the registration no. is allotted and a letter confirming Marketing authorization is issued. The normal time line for registration is about 18 months. The registration fees per product is 250 US dollar.

Keywords: FDA, Drug Act, marketing authorization, Veterinary products.

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References

1. Food and Drug Administration, Thailand
[Internet]. Thailand: FDA; [cited 2016 Feb 12]. Available from:
www.fda.moph.go.th/eng/drug/laws.stm
2. Code of Practice For Control Of The Use Of Veterinary Drugs in Thailand. [Internet]. Bangkok: Royal Gazette Vol.126 Special Section 187D; 2009 Dec 28 [cited 2016 Feb 11]. Available from:
www.acfs.go.th/standard/download/eng/veterinary_drugs.pdf
3. The drug Act B.E. 2510 (1967) [Internet]. Thailand: Thailaws.com; 1967 [cited 2016 Feb 13].
Available from:
www.thailaws.com/law/t_laws/tlaw0071_1.pdf
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How to Cite
Gupta, R. “MARKETING AUTHORIZATION OF VETERINARY PRODUCTS IN THAILAND”. International Journal of Drug Regulatory Affairs, Vol. 4, no. 1, Feb. 2018, pp. 21-23, doi:10.22270/ijdra.v4i1.178.