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