Generate higher-quality evidence with a stronger infrastructure on which to build and conduct studies, simplifying research for sponsors, participants and sites. Our software, analytics and participant-centric digital tools – such as eConsent and ePROs – are designed to transparently collect the right data, while upholding rigorous privacy and governance standards.
Accelerate your research with rich and diverse datasets that have greater length, depth and breadth in specific therapeutic areas. Long-term engagement models, participant-centered design and novel data sources enable prospective data capture over time, while upholding high quality, compliance, scientific and privacy standards.
Rapidly achieve your clinical trial recruitment goals with confidence through data-driven, participant-centric tools and services.
Advance your precision biomedical research and accelerate scientific breakthroughs by utilizing collaborative workspaces with compliance control.
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Alleviate research gridlock for your enterprise study sites through advanced, intuitive CTMS features that improve the simplicity, quality and cost-impact of research. This includes proprietary CTMS technology that configures PDF protocols into digitized workflows to free up your teams and power operations.