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