Signant Biotech Signant SmartSignals® Unified Platform EDC/DDC Comprehensive EDC/DDC solution with a 30-year track record, backed by the global reach and resources of Signant Biotech. 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. DOWNLOAD BROCHURE 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 unimportant. Our project managers and support teams are on your side. Why choose Signant’s EDC/DDC? 1. Rapid implementation 2. Flexible configuration for simple and complex studies alike 3. No-coding study design 4. Comprehensive library of eCRFs, edit checks, and custom functions 5. Leading UI and workflow management 6. No downtime 7. Seamless mid-study changes, with site-level versioning 8. Remote monitoring/remote SDV 9. Facilitates risk-based and targeted monitoring 10. Fully mobile-enabled with responsive design 11. Direct data capture 12. Ease of integration 13. Local and central lab data integration 14. Central coding 15. Standard, custom, and ad hoc reporting 16. Secure, clean data 17. Experienced and attentive project team 18. Available as full-service and self-service options 19. Part of a single, unified platform including eConsent, Telemedicine, RTSM, and ePRO Frequently Asked Questions 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. Connect With Us
Comprehensive EDC/DDC solution with a 30-year track record, backed by the global reach and resources of Signant Biotech.
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.
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.
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.
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 unimportant. Our project managers and support teams are on your side.
1. Rapid implementation 2. Flexible configuration for simple and complex studies alike 3. No-coding study design 4. Comprehensive library of eCRFs, edit checks, and custom functions 5. Leading UI and workflow management 6. No downtime 7. Seamless mid-study changes, with site-level versioning 8. Remote monitoring/remote SDV 9. Facilitates risk-based and targeted monitoring 10. Fully mobile-enabled with responsive design
11. Direct data capture 12. Ease of integration 13. Local and central lab data integration 14. Central coding 15. Standard, custom, and ad hoc reporting 16. Secure, clean data 17. Experienced and attentive project team 18. Available as full-service and self-service options 19. Part of a single, unified platform including eConsent, Telemedicine, RTSM, and ePRO