Verta Life Science consultants have successfully led chemical development activities on numerous projects from the identification, development and implementation of synthetic processes for the manufacture of active pharmaceutical ingredients (APIs), through to commercial supply.

Our experience covers the breadth of the drug development process, from laboratory based manufacture of early clinical supplies, through validation of processes in commercial manufacturing facilities.

We encourages application of a pragmatic (differentiated-development) approach to supporting early phase clinical development; while applying a systematic (Quality-by-Design) approach to the later phases of the development process.

On behalf of our clients we work with contract manufactures world wide to ensure the successful tech transfer and supply of APIs