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