Product Overview
Ease of understanding for patients. Full visibility and automated control over the consent process for sponsors. Extend your clinical trial command and control center with Suvoda eConsent.
Improve patient comprehension. Reduce site burden. And decrease regulatory risk, delays, and expenses created by mid-trial consent requirements.
In today’s clinical studies for novel, life-changing therapeutics, informed consent isn’t just a first step in a patient’s trial journey. It is central to a patient’s understanding of study procedures and is a critical ethical requirement. And it is a process that must be repeated along the way, as the vast majority of protocol amendments require the patients to re-consent. The result is heightened risk of patient misunderstanding, regulatory non-compliance, heavier administrative burden, and increased study expense and duration.
When approximately 70% of the oncology studies we support have at least one protocol amendment, the patient experience and sponsor visibility of Suvoda eConsent make it a must-have tool for study and site teams—and their patients.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Powerful features that drive patient understanding and reduce regulatory risk.
Suvoda eConsent features robust functionality that gives patients the tools they need to understand study information, which often includes complex medical and legal terms and concepts. At the same time, the visibility over consent across all study sites and patients means sponsors have control over the full process to minimize delays and reduce the risk of a regulatory finding.
Patient Comprehension
- Embedded videos and FAQs
- In-document discussion threads
- Cross-linked glossary
Flexible Design
- Electronic signature, wet ink upload, or print-and-sign consent
- Can accommodate multiple consent types (subject, caregiver, legally authorized representative)
- Multilingual capability
- Available on multiple devices — web-based, on-site, or patient device
About the company
Suvoda is a global clinical trial technology company dedicated to supporting complex studies for life-sustaining therapies. Seamlessly manage mission-critical, time-sensitive, and deeply-human interactions with the Suvoda Platform—a purpose-built, easy-to-use ecosystem delivering eConsent, IRT, eCOA, and ePatient.
Set up your clinical trial technology exactly as your study needs it, with simplified integrations, tools to remember your trial standards, and rapid deployment. Once launched, you’ll find the Suvoda Platform enhances the experience of moving through a study, for your team, your site professionals, and your patients alike. So everyone can confidently contribute to their clinical trial more easily than ever.
