In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard Drug Master File in Korea (All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard. The MFDS reviews the All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard KDMF as part of the drug registration process and uses the information provided in the All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard KDMF to evaluate the safety and efficacy of the drug.
After submitting a All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) 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 All-rac-alpha-tocopheryl acetate for peak identification, European Pharmacopoeia (EP) Reference Standard API can apply through the Korea Drug Master File (KDMF).
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