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