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