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