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