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