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, United States Pharmacopeia (USP) Reference Standard Drug Master File in Korea (Alpha Tocopheryl Acetate, United States Pharmacopeia (USP) Reference Standard KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Alpha Tocopheryl Acetate, United States Pharmacopeia (USP) Reference Standard. The MFDS reviews the Alpha Tocopheryl Acetate, United States Pharmacopeia (USP) Reference Standard KDMF as part of the drug registration process and uses the information provided in the Alpha Tocopheryl Acetate, United States Pharmacopeia (USP) Reference Standard KDMF to evaluate the safety and efficacy of the drug.
										After submitting a Alpha Tocopheryl Acetate, United States Pharmacopeia (USP) Reference Standard 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, United States Pharmacopeia (USP) Reference Standard API can apply through the Korea Drug Master File (KDMF).
										click here to find a list of Alpha Tocopheryl Acetate, United States Pharmacopeia (USP) Reference Standard suppliers with KDMF on PharmaCompass.