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