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