1. Total impurity profiling of APIs and finished dosage forms which includes development and validation of specific analytical methods, forced degradation studies etc.
2. Development and validation of analytical method for estimation of residual solvents and OVIs.
3. Particle sizing techniques.
4. Technical evaluation of inhalation products - MDIs/DPIs.
5. Also our experienced Bioanalytical scientist are skilled in Method  Development, Method Optimization, Method Validation and Application of these methods to the Analysis of Drugs in samples from BA/BE studies.
6. Bioavailability/Bioequivalence Projects involving pharmaceutical evaluation and adhering to international standards.

Thanks to its state-of-the-art facilities and competent technical staff, many overseas customers for tie-up and Joint ventures are now approaching SITEC.