Develop a solution to optimise the safety, efficacy and eventual regulatory success of your drug development.

SAPRO taps into an array of experienced and practicing physicians that can provide oversight on all medical aspects of your clinical trial, ensuring participant safety and data integrity. The team can also coordinate the necessary safety review meetings, safe-guarding the well-being of participants and maintaining the scientific validity of the study.

We have a dedicated expert available to Oncology studies.

ARGUS software if also offered.