In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Flagyl, Filmet Drug Master File in Korea (Flagyl, Filmet KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Flagyl, Filmet. The MFDS reviews the Flagyl, Filmet KDMF as part of the drug registration process and uses the information provided in the Flagyl, Filmet KDMF to evaluate the safety and efficacy of the drug.
After submitting a Flagyl, Filmet 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 Flagyl, Filmet API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Flagyl, Filmet suppliers with KDMF on PharmaCompass.