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