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