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