Bioequivalence study designs for generic solid oral anticancer drug products: Scientific and regulatory considerations
Article first published online: 21 SEP 2013
© 2013, The American College of Clinical Pharmacology
The Journal of Clinical Pharmacology
Volume 53, Issue 12, pages 1252–1260, December 2013
How to Cite
Kaur, P., Chaurasia, C. S., Davit, B. M. and Conner, D. P. (2013), Bioequivalence study designs for generic solid oral anticancer drug products: Scientific and regulatory considerations. Journal of Clinical Pharma, 53: 1252–1260. doi: 10.1002/jcph.163
- Issue published online: 14 NOV 2013
- Article first published online: 21 SEP 2013
- Accepted manuscript online: 28 AUG 2013 07:29AM EST
- Manuscript Accepted: 13 AUG 2013
- Manuscript Received: 8 MAY 2013
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