Stability testing and storage:
25°C ± 2°C / 60% RH ± 5%
30°C ± 2°C / 65% RH ± 5%
40°C ± 2°C / 75% RH ± 5%

Finished product and QC testing

Degradation Studies

Dissolution and physical testing

Method Development and Validation in accordance with ICH guidelines

Comprehensive Support for Formulation development

Environmental Monitoring for pharmaceutical actives and organics

Cleaning validation/verification

Drug substance and drug product testing

MS Structural Analysis

OVI and Residual Solvent testing