Simple tools to enhance patient engagement
Striving to make the clinical trial journey as simple as it can be, we design tools that are easy to use.
Our electronic informed consent solution allows patients to read crucial information at their own pace, and our electronic patient-reported outcome (ePRO) reduces the burden for them by collecting data points remotely.
Not only does this make life easier for patients, but it also increases engagement and delivers data in real time – leading to greater accuracy and faster decisions.
Improve communication, minimize disruption
Patients who participate in clinical trials lead their everyday lives outside the trial setting, balancing personal, work, and family commitments.
To ensure they can seamlessly engage with the study, tools like ePRO and eConsent play a critical role – streamlining communication and allowing patients to provide timely feedback and consent without added burdens.
Sectors
Pharma
Biotech
CRO
Medical device
Academia
