In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a all cis-5,8,11,14,17-Icosapentaenoic Acid Drug Master File in Korea (all cis-5,8,11,14,17-Icosapentaenoic Acid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of all cis-5,8,11,14,17-Icosapentaenoic Acid. The MFDS reviews the all cis-5,8,11,14,17-Icosapentaenoic Acid KDMF as part of the drug registration process and uses the information provided in the all cis-5,8,11,14,17-Icosapentaenoic Acid KDMF to evaluate the safety and efficacy of the drug.
After submitting a all cis-5,8,11,14,17-Icosapentaenoic 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 all cis-5,8,11,14,17-Icosapentaenoic Acid API can apply through the Korea Drug Master File (KDMF).
click here to find a list of all cis-5,8,11,14,17-Icosapentaenoic Acid suppliers with KDMF on PharmaCompass.