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