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ICH Harmonised Tripartite Guideline, International Conference on Harmonisation of Technical Requirements For Registration of Pharmaceuticals For Human Use, Validation of Analytical Procedures: Text and Methodology Q2(R1), (2005) Accessed date: April 2024 US Food and Drug Administration, M10 Bioanalytical Method Validation and Study Sample Analysis, (2022), Accessed date: April 2024 Pena-Pereira F, Wojnowski W, Tobiszewski M (2020) AGREEAnalytical GREEnness Metric Approach and Software