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