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