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