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