In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 094CADDB-59BF-4EDF-B278-59791B203EA2 Drug Master File in Korea (094CADDB-59BF-4EDF-B278-59791B203EA2 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 094CADDB-59BF-4EDF-B278-59791B203EA2. The MFDS reviews the 094CADDB-59BF-4EDF-B278-59791B203EA2 KDMF as part of the drug registration process and uses the information provided in the 094CADDB-59BF-4EDF-B278-59791B203EA2 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 094CADDB-59BF-4EDF-B278-59791B203EA2 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 094CADDB-59BF-4EDF-B278-59791B203EA2 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 094CADDB-59BF-4EDF-B278-59791B203EA2 suppliers with KDMF on PharmaCompass.