- Analytical method development on LC MS/MS, HPLC, GC and other sophisticated instruments.
- Analytical Method Validation as per ICH guidelines.
- Real-time and accelerated stability studies as per ICH guidelines.
- Analysis of bulk actives, intermediates and pharmaceuticals.
- Analysis of organic volatile impurities by GC-HS MS.
- Particle size analysis and test for crystallinity by optical microscopy.
- In vitro dissolution and drug release studies for conventional and modified release formulations.
- Product development and optimization of existing formulations.
