In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a C6H12O6.H2O Drug Master File in Korea (C6H12O6.H2O KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C6H12O6.H2O. The MFDS reviews the C6H12O6.H2O KDMF as part of the drug registration process and uses the information provided in the C6H12O6.H2O KDMF to evaluate the safety and efficacy of the drug.
After submitting a C6H12O6.H2O 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 C6H12O6.H2O API can apply through the Korea Drug Master File (KDMF).
click here to find a list of C6H12O6.H2O suppliers with KDMF on PharmaCompass.