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