*Method development/validation for identification of candidate new drugs and metabolites using HPLC and LC/MS, characterize metabolite formation and metabolic profiles of candidate drug using in vivo and vitro metabolism studies and drug-drug interaction studies, pharmacokinetic/toxicokinetic studies, metabolite ID, structure elucidation, advanced extraction techniques, pre-treatment of biological sample
*Writing/revising SOP, Test Method and Protocol according to GLP guideline

*Method development/validation in HPLC and LC/MS analysis for pharmaceutical compounds and their metabolites, degradants and impurities in different matrices; Assay and impurity for API in manufacture product, intermediate, in-process samples and raw material
*Method development/validation in HPLC and LC/MS analysis of biological fluid samples for bimolecular analysis, metabolite structure elucidation, pharmacokinetic/toxicokinetic studies, advanced extraction techniques,
*Train scientists/chemists (including a new QC manager) on analytical research and cGMP and GLP Compliance
*Writing/revising SOP, Test Method and Protocol according to CGMP, GLP and ICH guideline

*Method development/validation in HPLC and LC/MS analysis of biological fluid samples for bimolecular analysis, metabolite structure elucidation, pharmacokinetic/toxicokinetic studies, advance extraction techniques, pre-treatment of biological sample
*Assay and impurity for API in manufacture product, intermediate and raw material
*Protein in feed and biological sample, pesticide residue in plant and feed
*Train scientists/chemists on analytical research and GLP Compliance
*Writing/revising SOP, Test Method and Protocol according to GLP guideline

Analytical Chemistry

Analytical Chemistry

Physical Chemistry