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