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