Our Services

- Support to Analytical method development for Active Pharmaceutical ingredient and Formulation Dosage form.


- Impurity characterization


- De-formulation studies (Q1 and Q2).


- Laboratory Setup for regulatory markets.


- Method validation.


- Supports for Regulatory audits (USFDA, WHO….)

- Co - ordination for stability studies.


- Impurity Profiling Study, Drug Degradation Pathways.


- Innovator product characterization.


- GAP Analysis study.


- GLP Training.


- Industrial Training on Analytical Instruments.