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Volume 2013 (2013), Article ID 572170, 6 pages
Development and Validation of RP-HPLC Method for Azilsartan Medoxomil Potassium Quantitation in Human Plasma by Solid Phase Extraction Procedure
Department of Chemistry, Saurashtra University, Rajkot 36005, India
Received 21 June 2013; Accepted 14 August 2013
Academic Editors: I. P. Gerothanassis, B. Liu, and S. Pandey
Copyright © 2013 Paras P. Vekariya and Hitendra S. Joshi. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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- “Guidance for industry: bio analytical method validation,” US Department of Health and Human Services, Food and Drug Administration, CDER, Rockville, Md, USA, May 2001, http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm070107.pdf.