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