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