Analytical Development and Validation

Characterization of API, Excipients and Drug Product, Innovator

Stability indicating Method Development

Impurity Profiling

Dissolution Profiling

Residual Solvents analysis in API and Drug Products

Stability Protocol Preparation, Analysis & Monitoring - ICH

Method Validation – ICH/FDA

USP 467 – Residual solvents

Method Transfers

Standalone Analytical Services & Contract Stability Services