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