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