• API process development & scale-up
• Solid-state & formulation science
• Formulation development
• Excipients selection & compatibility
• Stability & shelf-life studies

Analytics & Bioanalytical Chemistry

• Analytics method development & validation(ICH Q2)
• Impurity profiling & quantitation
• Residual solvents & elemental impurities (ICH Q3C / Q3D)
• Dissolution, content uniformity, assay, potency
• Batch release testing, CoA, stability-indicating methods
• Specialized Routine Testing
• Enzyme activity assays (standardized QC panels)
• Heparin potency & purity testing
• Low Molecular Weight Heparin (LMWH) assays including Enoxaparin