In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Mettler-Toledo(R) Calibration substance ME 18872, Caffeine Drug Master File in Korea (Mettler-Toledo(R) Calibration substance ME 18872, Caffeine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Mettler-Toledo(R) Calibration substance ME 18872, Caffeine. The MFDS reviews the Mettler-Toledo(R) Calibration substance ME 18872, Caffeine KDMF as part of the drug registration process and uses the information provided in the Mettler-Toledo(R) Calibration substance ME 18872, Caffeine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Mettler-Toledo(R) Calibration substance ME 18872, Caffeine 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 Mettler-Toledo(R) Calibration substance ME 18872, Caffeine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Mettler-Toledo(R) Calibration substance ME 18872, Caffeine suppliers with KDMF on PharmaCompass.