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