Áų̀²Êͼ¿â±¦µä eConsent
Empowering Patients Right From?the?Start
What is eConsent for clinical trials? eConsent allows patients to understand trial objectives while providing consent through multimedia technology onsite or remotely.
Áų̀²Êͼ¿â±¦µä¡¯s eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials. Whether onsite or remote, Áų̀²Êͼ¿â±¦µä eConsent automates the patient enrollment process and onboards patients directly into Rave EDC, improving overall consent tracking management, reducing informed consent errors, and easing the administrative burden for sites and study teams. It also enhances the patient experience with easy-to-understand clinical trial information while improving participant compliance and boosting patient engagement.
The Value of Áų̀²Êͼ¿â±¦µä eConsent
Create a Better Patient Experience
Áų̀²Êͼ¿â±¦µä eConsent advances patient compliance and retention while enabling an increased understanding of study objectives, risks, benefits, and responsibilities. Our dedicated Patient Cloud Helpdesk optimizes the site and patient experience when and where you need it most.
Unified Platform Approach
Áų̀²Êͼ¿â±¦µä eConsent comes unified with the Áų̀²Êͼ¿â±¦µä Platform, the platform already used by the majority of the clinical trials in the world. While our competitors may be compatible with the Áų̀²Êͼ¿â±¦µä Platform, integration is not simplification.
Path to Hybrid & Fully Decentralized Studies
Part of the Patient Cloud suite of solutions, Áų̀²Êͼ¿â±¦µä¡¯s eConsent easily captures patient consent regardless of location while supporting 100% BYOD for added flexibility.
Key Features of Áų̀²Êͼ¿â±¦µä eConsent
Multiple Ways to Engage
Built with the ultimate flexibility in mind, patients in clinical trials can choose to provide consent at the site or remotely depending upon the design of the study.
Integrated with Rave EDC
Áų̀²Êͼ¿â±¦µä eConsent comes unified with the Áų̀²Êͼ¿â±¦µä Clinical Cloud, the platform already used by the majority of the clinical trials in the world. While our competitors may be compatible with the Áų̀²Êͼ¿â±¦µä Clinical Cloud, integration is not simplification.
User-Friendly Configuration Tools
Our clinical trial technology eliminates the need for developer support, customization, html conversion, and duplicate effort which helps to decrease eConsent study and site set-up timelines from months to weeks.
Related Solutions
Learn More
The Use of Electronic Informed Consent (eConsent) in a Blood Collection Study
A specialty division of a top ten pharma was preparing for an upcoming blood collection study, looking to recruit 6,000 patients spanning ten sites.
Moving away from their paper process, Áų̀²Êͼ¿â±¦µä eConsent modernized the clinical trial consenting process for patients, sites, and sponsors. Learn more about how Áų̀²Êͼ¿â±¦µä eConsent improved patient comprehension and reduced site workload.
Empowering Patients Right from the Start
Áų̀²Êͼ¿â±¦µä¡¯s eConsent is an innovative, patient-friendly, electronic informed consent and patient enrollment system for clinical trials. Built with the ultimate flexibility in mind, patients can choose to provide consent at the site or remotely depending upon the design of the study.
Electronic Informed Consent in Clinical Research
This white paper provides an overview of findings from the Áų̀²Êͼ¿â±¦µä eConsent study to understand the regulatory positions, adoption, and the variability regarding eConsent globally.