Determiniation and Validation of Alibendol using High Pressure Liquid Chromatography in Human plasma
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Song, Hyun-Ho
(Division of Bioequivalence, Korea Drug Test Laboratory)
Yu, Ji-Young (Division of Bioequivalence, Korea Drug Test Laboratory) Kim, Bo-Gyeom (Division of Bioequivalence, Korea Drug Test Laboratory) Park, Hyeon-Ju (Division of Bioequivalence, Korea Drug Test Laboratory) Choi, Kwang-Sik (Division of Bioequivalence, Korea Drug Test Laboratory) Kwon, Young-Ee (Division of Bioequivalence, Korea Drug Test Laboratory) |
1 | 식품의약품안전청 공고 제2009-289호. |
2 | Guidance for Industry, Bioanalytical Method Validation (2001), U.S. Department of Health and Human Services Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM). |
3 | Online Database of Chemicals from Around the World, chemBlink Inc. P.O. Box 5231 Cary, North Carolina 27512- 5231, The United States of America, http://www.chemblink.com/products/26750-81-2.htm. |
4 | 식품의약품안전청 의약품분야 사이버민원실, KFDA EZ drug, http://ezdrug.kfda.go.kr/. |
5 | 식품의약품안전청 고시 제2009-212호(2009.12.22, 개정), 의약품 재평가 실시에 관한 규정. |
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