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Medrio eConsent

Medrio eConsent

Medrio eConsent

Product catalog summary
Overview of Medrio's Consent Solution
Medrio's Consent solution is designed to streamline the consent process in clinical trials, enhancing patient comprehension and ensuring regulatory compliance. It supports both electronic and paper-based consent processes, offering flexibility to meet the needs of patients and clinical sites.
Key Features
  • Flexible Consent Technology: The solution improves participant comprehension and oversight by allowing consent through in-clinic tablet workflows or remotely via email and the MyMedrio portal.
  • Patient Experience Enhancement: The solution includes multimedia presentations, FAQs, and quizzes to improve understanding, and supports a BYOD model to focus on trial requirements.
  • Accelerated Setup and Changes: Consent forms can be uploaded to a tablet app for instant access, with easy control over consent versions and expedited re-consenting workflows.
  • Compliance and Oversight: Real-time access to consent progress data is provided, with centralized data management and robust patient data protection through encryption and permissions.
Medrio's Impact and Vision
Since 2005, Medrio has supported sponsors and CROs across various therapeutic areas and trial phases, contributing to over 375 regulatory approvals. The company emphasizes high-touch customer service and aims to reduce trial participation burdens while expecting rapid growth in eConsent adoption.
Contact Information
For more information, visit Medrio's website at www.medrio.com or contact them at +1 800.498.6830 or [email protected].
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Catalog excerpts

Medrio eConsent-1

SOLUTION SHEET Medrio eConsent Flexible consent technology improves participant comprehension and process oversight. The Consent Process Can Make or Break Your Study fail to retain enough patients of patients drop out of studies of those patients drop out due to a failure to understand study requirements 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 patient experience and the sites’ needs. Sites may either consent participants in-clinic using tablet-based workflows or remotely using email and MyMedrio, our secure participant portal

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Medrio eConsent-2

You’ve Got Options Unlike other Consent technology solutions, our fully integrated web-based Consent and EDC platform allows you to meet your study milestones by streamlining implementation and data collection. Multimedia presentations and participant quizzes enrich patient understanding. Plus, when time is of the essence, you can benefit from quick set-up options, including uploading IRBapproved paper consent documents. Improve Patient Experience M edrio’s BYOD model allows patients to focus on understanding the trial requirements, not on learning how to use a new device L everage in-clinic...

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