Comprehensive EDC/DDC solution with a 30-year track record,
backed by the global reach and resources of Signant Biotech
UNIFIED PLATFORM
EDC/DDC
A leading EDC/DDC solution for modern clinical trials
Modern clinical trials need simple yet comprehensive and agile EDC capabilities. From mobile-enablement for eSource collection at site and during decentralized home visits to remote source data verification (SDV) capabilities that reduce travel requirements for CRAs, our EDC/DDC provides these and more.
Four reasons customers
love our EDC/DDC
Whether using our full-service option or building your own EDC studies using self-service, our customers love our EDC/DDC solution
Ease of Use
Sites love our intuitive interfaces which make it easy to get their jobs done and clearly direct them to the next activities needed. Sponsors love the CRA workflow directions and convenient integration capabilities. Self-service users love our easy-to-use, no-coding design interface as well as the extensive library of eCRFs, edit checks, and custom functions provided out-of-the-box.
Flexibility
Our no-coding EDC accommodates both simple and highly complex study designs. Even the most complex oncology study with undefined numbers of cycles, and different cycle lengths across study arms, can be easily accommodated.
Exceptional Service
Full-service and self-service customers are delighted by our attentive service. We do the heavy lifting, leaving your team to focus on other aspects of study start-up. No customer is too small, and no question is unimportant. Our project managers and support teams are on your side.
Efficiency
Study set-up in 4-6 weeks (usually less), and no downtime when rolling out protocol amendments.
Why choose Signant’s EDC/DDC?
Study Set Up & Configuration
- Flexible configuration for simple and complex studies alike
- No-coding study design
- Part of a single, unified platform including eConsent, Telemedicine, RTSM, and ePRO
- Seamless mid-study changes, with site-level versioning
- Comprehensive library of eCRFs, edit checks, and custom functions
Data Collection & Management
- Rapid implementation
- Direct data capture
- Local and central lab data integration
- Central coding
- Secure, clean data
Monitoring & Quality Control
- Remote monitoring/remote SDV
- Facilitates risk-based and targeted monitoring
- Experienced and attentive project team
Streamlined Solutions
- Leading UI and workflow management
- Fully mobile-enabled with responsive design
- Ease of integration
- Standard, custom, and ad hoc reporting
- Available as full-service and self-service options
Our EDC solution is part of a fully unified eClinical platform
FAQs
Are you an eSource EDC?
Yes, our EDC/DDC supports eSource data collection. Our solution is fully mobile enabled with a responsive design that enables clear and easy use on a tablet or smartphone – so investigators can use the solution during on-site consultations, and nurses can use it during home visits. Our solution enables the genealogy of data to be clearly identified – making it easy to distinguish data that is eSource and data that has been transcribed.
Do you have an eCRF library?
Yes, our EDC/DDC comes with a comprehensive library of eCRFs, edit checks and custom functions. Our library speeds study builds by our project team, but the full library is also provided to self-service customers.
Do you support remote SDV?
Yes. Sites are able to upload source data evidence for remote review and sign off by the CRA. This speeds SDV activity, and reduces the amount of travel time CRAs need to expend.
Do you build EDC studies for us?
Yes, at Signant we offer both full service and self-service EDC options.
Can your EDC/DDC work alongside RBQM solutions?
Yes, our EDC/DDC makes it easy to define risk-based approaches to SDV, and to adjust these at the click of a button as the study progresses and the risk profile of each individual site is understood.
Want to learn more?
Get in touch with us for a solution tour and to discuss your data capture strategy