QbD-oriented development and validation of a bioanalytical method for nevirapine with enhanced liquid-liquid extraction and chromatographic separation-Reference-Cited by-同舟云学术

QbD-oriented development and validation of a bioanalytical method for nevirapine with enhanced liquid-liquid extraction and chromatographic separation

Published:2015-10-12 Issue:6 Volume:30 Page:818-828
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomed. Chromatogr.

Author:

Beg Sarwar¹,Chaudhary Vandna¹,Sharma Gajanand¹²,Garg Babita¹,Panda Sagar Suman³,Singh Bhupinder¹

Affiliation:

1. University Institute of Pharmaceutical Sciences, UGC Centre of Advanced Studies; Panjab University; Chandigarh 160 014 India

2. Formulation Research and Tech Transfer; IPCA Laboratories Limited; Kadhivali (W) Mumbai 400 067 India

3. Department of Pharmaceutical Analysis and Quality Assurance; Roland Institute of Pharmaceutical Sciences; Berhampur Odisha 760 010 India

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

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3. Development and validation of a stability-indicating liquid chromatographic method for estimating olmesartan medoxomil using quality by design;Beg;Journal of Chromatographic Science,2015

4. Quality by design (QbD) in analytical sciences: an overview;Bhutani;Pharma Times,2014

5. Chromatographic Methods

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