In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 04079A1RDZ Drug Master File in Korea (04079A1RDZ KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 04079A1RDZ. The MFDS reviews the 04079A1RDZ KDMF as part of the drug registration process and uses the information provided in the 04079A1RDZ KDMF to evaluate the safety and efficacy of the drug.
After submitting a 04079A1RDZ 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 04079A1RDZ API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 04079A1RDZ suppliers with KDMF on PharmaCompass.