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