1. G.P. Martin, K.L. Barnett, C. Burgess, P.D. Curry, J. Ermer, G.S. Gratzl, J.P. Hammond, J. Herrmann, E. Kovacs, D.J. LeBlond, R. LoBrutto, A.K. McCasland-Keller, P.L. McGregor, P. Nethercote, A.C. Templeton, D.P. Thomas, ML.J. Weitzel; Lifecycle Management of Analytical Procedures: Method Development, Procedure Performance Qualification, and Procedure Performance Verification; USP Pharmacopeial Forum 39(5) (2014) (available at https://www.uspnf.com/pharmacopeial-forum, accessed June 28, 2021).
2. In-Process Revision <1220> Analytical Procedure Life Cycle; USP Pharmacopeial Forum 46(5) (2020) (available at https://www.uspnf.com/pharmacopeial-forum, accessed June 28, 2021).
3. International Council on Harmonisation; Final Concept Paper ICH Q14: Analytical Procedure Development (2018) (available at https://ich.org/page/quality-guidelines, accessed June 28, 2021).
4. A Robust QBD Based High-Performance Thin-Layer Chromatographic Method for the Estimation of Aspirin, Clopidogrel Bisulphate and Rosuvastatin Calcium in a Pharmaceutical Formulation Using Experimental Design;Sankar;Curr. Anal. Chem.,2017
5. Application of Quality by Design in the Development of HPTLC Method for Estimation of Anagliptin in Bulk and inhouse Tablets;Patil;Eurasian J. Anal. Chem.,2017