In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a AZELAIC ACID, 95% Drug Master File in Korea (AZELAIC ACID, 95% KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AZELAIC ACID, 95%. The MFDS reviews the AZELAIC ACID, 95% KDMF as part of the drug registration process and uses the information provided in the AZELAIC ACID, 95% KDMF to evaluate the safety and efficacy of the drug.
After submitting a AZELAIC ACID, 95% 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 AZELAIC ACID, 95% API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AZELAIC ACID, 95% suppliers with KDMF on PharmaCompass.