In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide Drug Master File in Korea (5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide. The MFDS reviews the 5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide KDMF as part of the drug registration process and uses the information provided in the 5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide KDMF to evaluate the safety and efficacy of the drug.
After submitting a 5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their 5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 5-methyl-N-(4-(trifluoromethyl)phenyl)isoxazole-4-carboxamide suppliers with KDMF on PharmaCompass.