Oncology-Focused eCOA That Goes Beyond Reliable Tech
High-quality, reliable data to support regulatory decision-making and labelling
Ready to revolutionize the way you conduct oncology trials? Get started today.
Rapid eCOA builds using our solution’s intuitive and collaborative design interface
Enhanced patient experience with built-in patient engagement features
Flexibility to capture data at home or at site to ensure optimal measurement strategy
Develop an eCOA measurement strategy that meets FDA requirements on measure specificity and schedule of administration
Work with scale authors to adapt sub-scales to derive more disease-specific measures
Optimize eCOA schedule of events to minimize patient completion burden
Enable new scale development using item banks
Oncology research today demands flexible, scalable data capture solutions as well as considerations to minimize participant and site burdens. Discover how Signant SmartSignals eCOA, backed by 20 years of oncology and eCOA science expertise, enables study teams to meet changing regulatory requirements and generate reliable clinical evidence at any scale while optimizing trial participation and conduct.
Signant has provided eCOA support in 27% of the novel oncology drugs approved by the FDA and the EMA in the US and EU over the last 6 years.