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