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