In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a CC-4047, Actimid, 19171-19-8 Drug Master File in Korea (CC-4047, Actimid, 19171-19-8 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CC-4047, Actimid, 19171-19-8. The MFDS reviews the CC-4047, Actimid, 19171-19-8 KDMF as part of the drug registration process and uses the information provided in the CC-4047, Actimid, 19171-19-8 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CC-4047, Actimid, 19171-19-8 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 CC-4047, Actimid, 19171-19-8 API can apply through the Korea Drug Master File (KDMF).
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