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