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