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