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