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