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