[2]
Borman, P; Elder, D. Q2 (R1) validation of analytical procedures. ICH Quality guidelines, 2017, 5, 127-66.
[3]
Narang, A.S.; Boddu, S.H. Excipient Applications in Formulation Design and Drug Delivery. In: Excipient Applications in Formulation Design and Drug Delivery; Springer: Cham, 2015; pp. 1-10.
[15]
Chawla, R.K.; Gudhanti, S.N.; Kul, U.; Alavala, R.R. Development and validation of an inductively coupled plasma mass spectrometry method for estimation of elemental impurities in calcium acetate active pharmaceutical ingredient. Indian J. Pharm. Sci., 2021, 83(4), 830-837.
[16]
Sen, I; Shrivastava, D; Aggarwal, M; Khandal, RK Development of a validated method for quantitative analysis of heavy metals in herbal medicines using inductively coupled plasma mass spectrometry., 2021, 1, 487-502.
[17]
Diehl, B. Principles in NMR Spectroscopy. In: NMR Spectroscopy in Pharmaceutical Analysis;; Elsevier: Amsterdam, 2008; pp. 1-41.
[21]
Khan, FN; Baig, MS; Nihalani, G; Imran, M; Deshingkar, N Formulation of generic atorvastatin calcium tablet by reverse engineering technique.,
[30]
Kumssa, L.; Layloff, T.; Hymete, A.; Ashenef, A. High performance thin layer chromatography (HPTLC) method development and validation for determination of doxycycline hyclate in capsule and tablet formulations. Acta Chromatogr., 2021, 34(3)
[31]
Ambati, P; Bala Krishna, P; Srinivasa Rao, Y; Varaprasada Rao, K; Deepthi, R. Instrumentation and future prospects of HPTLC-a.,
[44]
Gas Chromatography; Poole, C., Ed.; Elsevier: Amsterdam, 2012.
[64]
Verma, G.; Mishra, M. Development and optimization of UV-Vi’s spectroscopy–A review. World J. Pharm. Res., 2018, 7(11), 1170-1180.
[65]
Jani, B.R.; Shah, K.V.; Kapupara, P.P. Development and validation of UV spectroscopic first derivative method for simultaneous estimation of dapagliflozin and metformin hydrochloride in synthetic mixture. J Bioequivalent., 2015, 1(1), 102.
[68]
Nataraj, K.S.; Charya, S.R.; Goud, E.S.; Ramanjineyulu, S.S. Simple quantitative method development and validation of valsartan in pure form and pharmaceutical dosage forms by UV–spectroscopy. Int. J. Pharma Bio Sci., 2011, 1(2)
[70]
Kulkarni, A.A.; Vaidya, I.S. Flow injection analysis: An overview. J Crit Rev., 2015, 2, 19-24.