Experienced in guiding pre-clinical research with a focus on in vitro and in vivo study design, pharmacological evaluation, and toxicological assessment. Skilled in selecting appropriate experimental models, dose optimization, and interpreting pharmacokinetic and pharmacodynamic data. Adept at developing scientifically robust protocols aligned with OECD and CPCSEA guidelines. Provides end-to-end support from study conceptualization to data analysis, ensuring reproducibility, ethical compliance, and high-quality outcomes. Strong emphasis on translational relevance to facilitate progression from laboratory research to clinical application.