1 |
Ministry of Food and Drug Safety (2014). Standard for pharmaceutical equivalence test, 2014-49, Ministry of Food and Drug Safety, Korea.
|
2 |
Chow, S. C. and Liu, J. (2008). Design and analysis of bioavailability and bioequivalence studies, Third edition, Chapman & Hall/CRC, New York.
|
3 |
Jeong, G. and Park, S. (2011). On evaluation of bioequivalence for highly variable drugs. The Korean Journal of Applied Statistics, 24, 1055-1076.
과학기술학회마을
DOI
ScienceOn
|
4 |
Noh, S. and Park, S. (2013). Some statistical considerations on 2 k crossover designs for bioequivalence trial. The Korean Journal of Applied Statistics, 26, 675-686.
과학기술학회마을
DOI
ScienceOn
|
5 |
Park, S., Nam, B., Chung, Y., Lee, J. and Jeong, G. (2010). Statistical considerations of the add-on test on bioequivalence trial. Communications for Statistical Applications and Methods, 17, 107-115.
과학기술학회마을
DOI
ScienceOn
|