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