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