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