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-docosa-4,7,10,13,16,19-hexaenoic acid Drug Master File in Korea (all-cis-docosa-4,7,10,13,16,19-hexaenoic acid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of all-cis-docosa-4,7,10,13,16,19-hexaenoic acid. The MFDS reviews the all-cis-docosa-4,7,10,13,16,19-hexaenoic acid KDMF as part of the drug registration process and uses the information provided in the all-cis-docosa-4,7,10,13,16,19-hexaenoic acid KDMF to evaluate the safety and efficacy of the drug.
After submitting a all-cis-docosa-4,7,10,13,16,19-hexaenoic 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-docosa-4,7,10,13,16,19-hexaenoic acid API can apply through the Korea Drug Master File (KDMF).
click here to find a list of all-cis-docosa-4,7,10,13,16,19-hexaenoic acid suppliers with KDMF on PharmaCompass.