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