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