Signant SmartSignals eConsent eConsent Ensure patient comprehension and audit-ready consent documentation Gain informed signatures Eliminate audit findings Unlike paper consent forms, our digital platform eliminates ambiguities as well as provides a fully transparent and traceable time/date stamped process. Ensure correct ICF versions You never have to worry about using older ICF versions – our consent solution takes care of it for you. Error-free re-consenting Streamline the re-consenting process to meet study amendments, at home or at site. OFTEN COMBINED WITH: eCOA > Patient Concierge > Sensors & Wearables > Telemedicine > Download Brochure Why choose Signant SmartSignals? 1 Simple SmartSignals eConsent simplifies patient consent for studies at any scale with the industry’s leading platform for remote or on-site consent. 2 Flexible The flexible platform facilitates patient-investigator discussions, accelerates mid-study reconsenting, and guarantees the correct versions are used at all times. 3 Robust From design to trial experience and document management, our robust SmartSignals eConsent solution lets participants make informed decisions and reduces burden for all. Signant SmartSignals Consent benefits everyone Participants Transforming the traditional paper consent form into an engaging digital experience, Signant SmartSignals eConsent supports various learning styles and checks comprehension. Sites & study collaborators Say goodbye to multiple devices and logins – our Signant SmartSignals eConsent can be deployed with our eCOA, RTSM, and Patient Concierge solutions. Sponsors The intuitive interface provides a real-time, interactive picture of study progress, while the complete audit trail minimizes regulatory risks. eConsent solutions to support any study At Signant, we provide solutions to best support your study. When it comes to eConsent, we give you the freedom to choose between a simplified, PDF-based consent form and a fully interactive, multimedia consent experience. All our eConsent options allow participants to learn study requirements at their own pace before they consent/reconsent. Best of all, each of our tiered eConsent options can be rapidly implemented and applied to on-site, virtual, or hybrid studies. Silver Try our simple and cost-effective PDF-based eConsent license with rapid implementation timelines. Gold This PDF-based eConsent license option offers additional functionalities such as version control, patient portal, remote monitoring dashboards, and electronic or paper signatures. Platinum By far our most advanced, comprehensive eConsent option, the Platinum license offers an engaging and rich digital patient experience. You’ll get template libraries, video support, dynamic reporting, as well as the ability to integrate with other solutions. This option is ideal for studies that need to obtain consent for lab sample collection, and for more complex studies where the use of multimedia, flagging content, and patient/site managed interactions are desired to improve patient understanding and experience. You choose your involvement level Our Gold or Platinum eConsent options are available in a self-service model, where you use your existing infrastructure to develop unique consent forms and documentation, and have complete control over the consent process. Need more guidance? Add on project delivery services and our experienced operational delivery team will manage the entire process for you. Ask us about our Design and Consultancy Services which support your team in a self-service model. Frequently Asked Questions What is clinical trial eConsent? Clinical trial eConsent (electronic informed consent) is a digital consent process that potential study participants undergo prior to enrollment as well as throughout the study to confirm their comprehension. eConsent may employ multiple electronic media to convey information related to the study and obtain informed consent. It can be used remotely or on site. What types of studies can be supported by eConsent? Our eConsent solutions can be used for traditional, site-based eConsent forms as well as remote, at-home consent forms. Signant’s tiered options support a wide range of clinical research studies – from Phase I studies to global Phase III studies. Why should clinical researchers transition from paper-based consent forms to eConsent forms? By switching from traditional forms to eConsent forms, sponsors can expect significant improvements, such as enhanced clinical data quality and traceability, minimized audit findings, real-time visibility and monitoring, increased site efficiencies, as well as a centralized document mangement. How can clinical trials improve compliance with eConsent? eConsent improves adherence in clinical trials by ensuring study participants sign the correct consent form version. It uses date and time stamps as well as real-time monitoring for better traceability. Does your eConsent solution offer data integration tools and clinical data exchange with other systems? Signant’s eConsent solution offers integration with our other clinical data solutions from our SmartSignal product suite, as well as with other eClinical systems. Want to learn more? Add eConsent to your study to manage the various consent forms more efficiently – contact our team today. Connect With Us
Eliminate audit findings Unlike paper consent forms, our digital platform eliminates ambiguities as well as provides a fully transparent and traceable time/date stamped process. Ensure correct ICF versions You never have to worry about using older ICF versions – our consent solution takes care of it for you. Error-free re-consenting Streamline the re-consenting process to meet study amendments, at home or at site.
SmartSignals eConsent simplifies patient consent for studies at any scale with the industry’s leading platform for remote or on-site consent.
The flexible platform facilitates patient-investigator discussions, accelerates mid-study reconsenting, and guarantees the correct versions are used at all times.
From design to trial experience and document management, our robust SmartSignals eConsent solution lets participants make informed decisions and reduces burden for all.
Participants Transforming the traditional paper consent form into an engaging digital experience, Signant SmartSignals eConsent supports various learning styles and checks comprehension. Sites & study collaborators Say goodbye to multiple devices and logins – our Signant SmartSignals eConsent can be deployed with our eCOA, RTSM, and Patient Concierge solutions. Sponsors The intuitive interface provides a real-time, interactive picture of study progress, while the complete audit trail minimizes regulatory risks.
At Signant, we provide solutions to best support your study. When it comes to eConsent, we give you the freedom to choose between a simplified, PDF-based consent form and a fully interactive, multimedia consent experience. All our eConsent options allow participants to learn study requirements at their own pace before they consent/reconsent. Best of all, each of our tiered eConsent options can be rapidly implemented and applied to on-site, virtual, or hybrid studies.
This PDF-based eConsent license option offers additional functionalities such as version control, patient portal, remote monitoring dashboards, and electronic or paper signatures.
By far our most advanced, comprehensive eConsent option, the Platinum license offers an engaging and rich digital patient experience. You’ll get template libraries, video support, dynamic reporting, as well as the ability to integrate with other solutions. This option is ideal for studies that need to obtain consent for lab sample collection, and for more complex studies where the use of multimedia, flagging content, and patient/site managed interactions are desired to improve patient understanding and experience.
Our Gold or Platinum eConsent options are available in a self-service model, where you use your existing infrastructure to develop unique consent forms and documentation, and have complete control over the consent process. Need more guidance? Add on project delivery services and our experienced operational delivery team will manage the entire process for you. Ask us about our Design and Consultancy Services which support your team in a self-service model.
Add eConsent to your study to manage the various consent forms more efficiently – contact our team today.