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