With 85% of studies failing to retain enough patients, 30% of patients dropping out of studies, and 8% of those patients dropping out due to failure to understand study requirements, the consent process can make or break study success.
Medrio’s Consent solution empowers organizations to accelerate all aspects of the consent process, from setting up and modifying forms to ensuring patient comprehension, while remaining in full regulatory compliance.
Our flexible solution supports both electronic and paper-based processes, allowing you to prioritize the patients’ experience and the sites’ needs. Sites may either consent participants in-clinic using tablet-based workflows or remotely using email and Medrio’s secure Participant Portal.
Unlike other Consent technology solutions, our fully integrated web-based Consent and EDC platform allow you to meet your study milestones by streamlining implementation and data collection. Our solution supports optional multimedia presentations and participant quizzes to enrich patient understanding, and we know that when time is of the essence, quicker set-up options may be preferred. Our system also allows you to upload and use IRB-approved paper consent documents when timelines don’t allow for lengthy consent storyboarding and multiple IRB approval rounds.