̨ͼⱦ 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.

̨ͼⱦ䡯s eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials. Whether onsite or remote, ̨ͼⱦ 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 ̨ͼⱦ eConsent

Create a Better Patient Experience

̨ͼⱦ 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.

Greater Efficiency

Decrease study and site set-up timelines from months to weeks while eliminating significant delays and risks associated with HTML conversion. eConsent also delivers guaranteed signature compliance, remote consent monitoring, and site screening metrics.

Unified Platform Approach

̨ͼⱦ eConsent comes unified with the ̨ͼⱦ Platform, the platform already used by the majority of the clinical trials in the world. While our competitors may be compatible with the ̨ͼⱦ Platform, integration is not simplification.

Path to Hybrid & Fully Decentralized Studies

Part of the Patient Cloud suite of solutions, ̨ͼⱦ䡯s eConsent easily captures patient consent regardless of location while supporting 100% BYOD for added flexibility.

Key Features of ̨ͼⱦ eConsent

Multiple Ways to Engage

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

Integrated with Rave EDC

̨ͼⱦ eConsent comes unified with the ̨ͼⱦ Clinical Cloud, the platform already used by the majority of the clinical trials in the world. While our competitors may be compatible with the ̨ͼⱦ Clinical Cloud, integration is not simplification.

User-Friendly Configuration Tools

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.

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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, ̨ͼⱦ eConsent modernized the clinical trial consenting process for patients, sites, and sponsors. Learn more about how ̨ͼⱦ eConsent improved patient comprehension and reduced site workload.

Empowering Patients Right from the Start

̨ͼⱦ䡯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 ̨ͼⱦ eConsent study to understand the regulatory positions, adoption, and the variability regarding eConsent globally.

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