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