Analytical Testing & Development

Avista Pharma Solutions is a leading provider of comprehensive analytical testing and method development services. We offer best-in-class services for structural characterization, material characterization, elemental impurities analysis (per ICH Q3D, USP <232> and USP <233>), potential genotoxic impurities, impurity isolation and identification, DMPK analysis, method development and validation, raw material testing, API and Drug Product release testing and stability testing.


See what success looks like: Range Finding Studies,  Fate & Purge Studies, Qualified Reference StandardsOvercoming Limitations to Achieve Uniform Dosing, Mitigating Hidden Risks: Extractables and Leachables, Rapid Characterization of Impurities and Ruling Out Cross-contaminants: Rapid Delivery of a Validated Cleaning Method case studies.