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