Chemometrics‐assisted development of a liquid chromatography method for estimation of lapatinib in tablets: A case study on a novel quality concept

Author:

Panda Sagar Suman1ORCID,Bera Ravi Kumar Venkata Varaha1,Behera Aswini Kumar1,Beg Sarwar2ORCID

Affiliation:

1. Department of Pharmaceutical Analysis and Quality AssuranceRoland Institute of Pharmaceutical Sciences Berhampur Odisha India

2. Department of Pharmaceutics, School of Pharmaceutical Education & ResearchJamia Hamdard, Hamdard Nagar New Delhi India

Publisher

Wiley

Reference24 articles.

1. International Conference on Harmonization (ICH) of Technical Requirements for Registration of Pharmaceuticals for Human Use Topic Q9: Quality Risk Management (ICH Geneva Switzerland 2005).

2. Quality risk management (QRM) supported systematic development and validation of an UFLC method for determination of a novel anti‐PAH agent in pharmaceuticals;Panda S. S.;World J. Pharm. Res.,2018

3. Analytical lifecycle management approach: Application to development of a reliable LC method for estimation of lacidipine

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

5. Response surface methodology (RSM) as a tool for optimization in analytical chemistry

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