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