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