In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Policresulen 50% Drug Master File in Korea (Policresulen 50% KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Policresulen 50%. The MFDS reviews the Policresulen 50% KDMF as part of the drug registration process and uses the information provided in the Policresulen 50% KDMF to evaluate the safety and efficacy of the drug.
After submitting a Policresulen 50% 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 Policresulen 50% API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Policresulen 50% suppliers with KDMF on PharmaCompass.