- Process Research on novel multi-step synthetic routes
- Development and Optimisation of chemical processes for new drug candidates devoted to Clinical Trials
- Scale-up from Laboratory to GMP Kilo Lab, to GMP Pilot Productions and from Pilot to large scale commercial productions
- Analytical Methods Development and Validation
- Identification and isolation of impurities and degradation products
- Regulatory Support in the development of DMF's/CTD’s for advanced intermediates as well as for the final API’s
- Project feasibility study in 15 working days