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