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