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