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