Services     The Chao Center efficiently exceeds client expectations while providing cGMP compliant pharmaceutical development services including:     Formulation Development     Pre-Formulation Excipient Compatibility Studies Excipient Selection/Ratio Determination Modified/Sustained Released Dosage Brand Extension Formulation Formulation Development Schedule II-IV Drug Product Development     Analytical Development     Analytical Methods Development Method Validation Cleaning Studies and Validation USP/NF Testing Stability Testing (ICH Guidelines) In-Process Testing     Manufacturing both of clinical and commercial products including:     Tablets Capsules Semi-solids Syrups Suspensions Blinding Studies