There is a lot going on in any clinical study. Many research projects are funded by grants, which usually means a limited technology budget and a set duration to complete the project.

In addition, most research studies must follow specific protocols and maintain compliance with standards and regulations, including those required by HIPAA.

While easy access to study data and metrics should be available to study administrators, participant data must be protected and kept confidential. Because of these challenges, most research projects still operate via paper documentation or expensive custom in-house-built applications.

It’s been estimated that approximately 85% of complex studies are still managed on paper.

Interacting and retaining participants for the duration of the study is difficult in rural areas and large-scale studies.

Ensuring the integrity of data, protocol adherence and consistent processes are a struggle for multi-site study teams.

Onboarding of participants

Communication with sites and participants

Surveys to capture outcome data

Real-time analytics

Management of clinical activities and lab results

Calendar management for onsite or telemedicine visits

Improving retention and protocol compliance