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