Medidata -Model eConsent -Innovative, Regulatory-Compliant, Patient-Friendly, Electronic Consent System for Clinical Trials
Medidata’s eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials. Whether onsite or remote, Medidata 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.
Create a Better Patient Experience
Medidata 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
Medidata eConsent comes unified with the Medidata Clinical Cloud, the platform already used by the majority of the clinical trials in the world. While our competitors may be compatible with the Medidata Clinical Cloud, integration is not simplification.
Path to Hybrid & Fully Decentralized Studies
Part of the Patient Cloud suite of solutions, Medidata`s eConsent easily captures patient consent regardless of location while supporting 100% BYOD for added flexibility.
1. 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.
2. Integrated with Rave EDC
Medidata eConsent comes unified with the Medidata Clinical Cloud, the platform already used by the majority of the clinical trials in the world. While our competitors may be compatible with the Medidata Clinical Cloud, integration is not simplification.
3. 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.