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