Signant Health's Unified Platform delivers the perfect balance of power and simplicity - a comprehensive EDC solution that accelerates study timelines without sacrificing quality or compliance, with modular add-ons tailored to your study needs.
Simplified User Experience
- A single access point and a single set of user credentials enables access to our EDC and its add-on modules, eConsent, eCOA, TeleVisits and Randomization through a single URL and a single sign on
- Converged, guided workflow means users move invisibly between applications – simplifying the user experience
- Reduced site training requirements
- Reduced site burden means more time for mission-critical study activities and more time with patients
Rapid Setup
- A single configurable designer enables EDC implementation in just 4-6 weeks
- Highly-configurable, no-software-coding designer tools accelerate study builds
- A growing library of eCRFs with standard edit checks facilitates easy reuse
Self- or Full-Service Models
- A single, intuitive, no-software-coding designer enables Sponsors and CROs to easily design, configure, and put live their own studies; and apply seamless mid-study changes; all with minimal training
- Self- or full-service implementation models empower study teams to choose the best approach for their needs and goals
Expertise and Scale of Signant Health
- Science – Our experienced science and medicine, eCOA science, data management, and in-house biostatistics teams ensure optimal study design and best-practices are implemented
- Logistics – Where needed, our in-house logistics service ensures all sites and patients across the globe receive fully-configured and tested eCOA devices on time
- Translations and scale management – Signant experts work with eCOA scale authors and translation vendors to ensure right scales, with right versions, and reliable translations
- Site- and patient-facing helpdesk – Our 24/7, multilingual helpdesk ensures sites and patients have the support they need, when they need it
- A single access point and a single set of user credentials enables access to our EDC and its add-on modules, eConsent, eCOA, TeleVisits and Randomization through a single URL and a single sign on
- Converged, guided workflow means users move invisibly between applications – simplifying the user experience
- Reduced site training requirements
- Reduced site burden means more time for mission-critical study activities and more time with patients
- A single configurable designer enables EDC implementation in just 4-6 weeks
- Highly-configurable, no-software-coding designer tools accelerate study builds
- A growing library of eCRFs with standard edit checks facilitates easy reuse
- A single, intuitive, no-software-coding designer enables Sponsors and CROs to easily design, configure, and put live their own studies; and apply seamless mid-study changes; all with minimal training
- Self- or full-service implementation models empower study teams to choose the best approach for their needs and goals
- Science – Our experienced science and medicine, eCOA science, data management, and in-house biostatistics teams ensure optimal study design and best-practices are implemented
- Logistics – Where needed, our in-house logistics service ensures all sites and patients across the globe receive fully-configured and tested eCOA devices on time
- Translations and scale management – Signant experts work with eCOA scale authors and translation vendors to ensure right scales, with right versions, and reliable translations
- Site- and patient-facing helpdesk – Our 24/7, multilingual helpdesk ensures sites and patients have the support they need, when they need it
EDC
Our EDC module is a full-featured data capture solution with the ability to fully support modern trial designs including the option of eSource data capture, remote SDV, and risk-based monitoring support.
eCOA
Combining our EDC with our eCOA add-on module provides a consumer-grade patient experience and supports ePRO, eObsRO, and eClinRO capture both at site and at home.. Completion reminders and reporting drive on-time data collection, and biometric authentication simplifies the patient experience.
Randomization
Adding our Randomization module provides robust and reliable randomization and fully embedded within the EDC workflow. Combined with rapid and transparent emergency unblinding, this simplifies site staff activities and maintains trial integrity.
eConsent
Including our eConsent add-on module enables seamless transition from consenting to screening within site workflow. Simplifying the process of consent and reconsent, our module can be used for fully remote or on-site consenting.
TeleVisit
TeleVisits provides secure, compliant video connectivity between site and patient. Our add-on solution is optimized for low bandwidth operation, works on any web-enabled device, and supports ad-hoc and scheduled TeleVisit meetings.