The Analytical Chemistry group at VVP works closely with our Pre-Formulation and Stability Testing group to choose the correct form of a given drug substance, evaluate its physical and chemical properties, and assess the stability of the drug under various conditions to provide an optimal drug-delivery system.
The Analytical Chemistry group has the capacity to verify chemical structures and compound purity, develop and validate analytical methods to quantify drug substances and degradation products in formulations or biological samples, evaluate of pharmaceutical dosage forms according to USP requirements, and assess drug kinetics and pharmacodynamics.