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