A simple-to-use and rapid-to-implement, single, integrated eClinical platform that meets the needs of modern clinical trials
EDC/DDC
Our EDC/DDC module is a full-featured EDC 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
The eCOA module within our Unified Platform provides a consumer-grade patient experience, and supports ePRO, eObsRO and eClinRO capture at site and at home. Compliance reminders and reporting drive on-time completion, and biometric authentication simplifies the patient experience.
RTSM
The RTSM module built into our Unified Platform provides robust and reliable randomization and medication supply chain management, through simple and intuitive interfaces. Combined with depot and CMO integrations, RTSM drives efficient and transparent processes.
eConsent
The integrated eConsent module within our Unified Platform enables configurable workflow for consent and reconsent, including the incorporation of legally authorized representatives and witness signatures, and can be used for fully remote or on-site consenting.
Televisit
TeleVisits provides secure, compliant video connectivity between site and patient, that can be used alongside EDC, eConsent, and eCOA. It is optimized for low bandwidth operation, works on any web-enabled device, and supports ad-hoc and scheduled TeleVisit meetings.
Participant Tracker
With our integrated Participant Tracker, study teams get transparent management and oversight of pre-screening activity by providing sites with a single, central location to track and manage patient enrolment, including recruitment vendor integration.
Simplified User Experience
- A single access point and a single set of user credentials enables access to all platform components through a single URL and a single sign on, including EDC/DDC, eCOA, eConsent, RTSM, Participant Tracker, and TeleVisits
- 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 implementation in just 4-6 weeks
- Highly-configurable, no-software-coding designer tools accelerate study builds
- A growing library of eCRFs and eCOA measures, 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, and RTSM specialist 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
- 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 all platform components through a single URL and a single sign on, including EDC/DDC, eCOA, eConsent, RTSM, Participant Tracker, and TeleVisits
- 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 implementation in just 4-6 weeks
- Highly-configurable, no-software-coding designer tools accelerate study builds
- A growing library of eCRFs and eCOA measures, 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, and RTSM specialist 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
- Patient-facing helpdesk – Our 24/7, multilingual helpdesk ensures sites and patients have the support they need, when they need it