Product Overview
Accessible on any web-enabled device (BYOD or provisioned), our scalable solution can inform and consent participants anywhere in the world. Flexible enough for any country or site, you can easily collect compliant signatures (digital or wet-ink), on-site or remote with integrated TeleVisit.
Stay connected with your patients and their data. Real-time notifications help ensure compliance while patient and caregiver-friendly ePROs make it easy for sponsors to track toxicity and tolerability in real time.
Gain complete visibility and oversight into your trial with real-time monitoring of all consent activities within a single dashboard and ensure inspection-ready audit trails with fully integrated template management and version control.
- Self-service authoring tool to easily create engaging consent templates
- Biosample attribution to confirm storage permissions for consent objects
- Permission-based workflows by roles and responsibilities for secure control
- Designed to comply with all global regulations, including FDA 21 CFR Part 11, ICH E6 (R2), and GDPR
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
What's the difference between eConsent and Medable’s Total Consent?
While Total Consent is an eConsent tool at heart, it features additional functionality, such as wet-ink signature support, that enables it to be deployed worldwide, in any country conducting clinical research. In addition, capabilities like TeleVisit are built into Medable’s Total Consent and don’t require additional tools or login credentials. To learn more visit our Total Consent Management page.
Where does Total Consent work?
Total Consent can be used both in the clinic, at home, and anywhere where a trial participant has an internet connection across 60 different locales. Total Consent was designed to comply with all global regulations, including FDA 21 CFR Part 11, ICH E6 (R2), and GDPR. Medable’s Total Consent currently supports 115+ languages in over 60 countries.
Can I use Total Consent across multiple studies and different trial types?
Yes. Total Consent can scale to trials of all sizes, whether you need to deploy eConsent on one study or multiple studies. Our solution also provides more efficiency the more you use it by creating standardized delivery methods for your organization.
About the company
Discover the future of clinical research with eCOA solutions that streamline data collection, improve adherence, and deliver actionable insights—all powered by our comprehensive decentralized clinical trial (DCT) platform.
Informed by DCT experts, patient insights, and site feedback, the Medable platform accommodates the complex research landscape in an intuitive and simple user interface. Offered in over 60 countries and 120 languages, our cloud-agnostic, single API platform offers self-service build and a library of system integrations for maximum reach and scalability. Your study benefits from our extensive network of partners from retail pharmacy and site networks, data providers for RWE and LTFU, and direct-to-patient offering of connected sensors and home health providers.
