Analytical Method Development

In our cGMP compliant R & D laboratory, our experts develop and document the analytical methods in the following applications with HPLC, TLC, GC, DSC, FTIR and all the equipment needed

Potency evaluation
Dissolution (dissolution rate) studies
Impurity and related compounds
Moisture
Metal
Residue solvents
Physical and chemical tests
Cleaning management
DMF apps-updates Other customer-oriented tests
Drug stability tests In vitro-in vivo correlation (f2 and f1 assessments)
Our quality control team supports you in the following pharmaceutical development applications;
Non-traditional method applications
Pharmaceutical active substance (APIs) and auxiliaries, intermediates decontamination
In-process tests
Process validation design and validation tests
Finished product release and stability
Packaging-cap-cap tests