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