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