Validation of a dissolution method with HPLC analysis for lasofoxifene tartrate low dose tablets-Reference-Cited by-同舟云学术

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Validation of a dissolution method with HPLC analysis for lasofoxifene tartrate low dose tablets

Published:2007-09 Issue:5 Volume:44 Page:1064-1071
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Space J. Sean,Opio Alex M.,Nickerson Beverly,Jiang Hong,Dumont Monica,Berry Mark

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference14 articles.

1. ICH-Q2A Guideline for Industry, Text on Validation of Analytical Procedures, March 1995.

2. Guidance for Industry, Q2B Validation of Analytical Procedures: Methodology, November 1996.

3. Development and validation of a dissolution test for a once-a-day combination tablet of immediate-release cetirizine dihydrochloride and extended-release pseudoephedrine hydrochloride

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