Transforming Clinical Trials with IRT and eConsent: A New Era of Patient-Centric Research

Welcome to a revolutionary approach to clinical trials with Delve Health, where we seamlessly integrate eConsent technology and clinical trial IRT (Interactive Response Technology) to redefine the patient experience while optimizing data accuracy. Our mission? To empower patients, enhance compliance, and streamline operations—all while making clinical research more inclusive and efficient.

Who We Are
At Delve Health, we’re trailblazers at the intersection of healthcare innovation and technology. By combining eConsent solutions with the power of clinical trial IRT, we’re building a future where research is faster, smarter, and truly patient-focused.

Our advanced platforms make it easier for patients to provide informed consent from anywhere in the world while giving researchers the tools they need to track, randomize, and monitor trials in real time. Whether you’re managing a global trial or focusing on local research, we ensure every step of the process is simplified and compliant.

What is eConsent & Clinical Trial IRT?
eConsent (electronic informed consent): A fully digital, interactive method that ensures patients have a clear, multimedia-guided understanding of trial participation, risks, and benefits before consenting.
Clinical Trial IRT: A technology platform that automates and optimizes trial logistics, including patient randomization, inventory management, and real-time reporting. This ensures every aspect of the trial is smooth, efficient, and auditable.
By integrating these two solutions, Delve Health delivers unmatched efficiency, transparency, and patient satisfaction.

How Delve Health Combines eConsent and IRT
Interactive and Transparent Consent Forms
Our eConsent platform features videos, infographics, and interactive Q&A tools to help patients understand the trial in detail. Clear communication leads to better decision-making and trust.

Real-Time Randomization & Tracking
Using IRT, trial teams can randomize patients instantly, track their participation, and monitor trial supply chains—ensuring operations run smoothly without delays.

Remote Accessibility
Both eConsent and IRT platforms are accessible on smartphones, tablets, and computers, empowering patients to participate and stay informed from anywhere. This eliminates geographic barriers and fosters diversity in trials.

Enhanced Compliance & Documentation
With automated audit trails, our solutions guarantee regulatory compliance, reducing risks while improving transparency for stakeholders.

Real-Time Updates & Monitoring
Whether it’s a consent form revision or supply chain data, our platforms allow real-time updates, ensuring both patients and researchers always have the most accurate information.

Why eConsent & IRT are Game-Changers
Efficiency: Faster enrollment, reduced paperwork, and streamlined operations.
Patient Engagement: Multimedia tools improve patient understanding and satisfaction.
Global Reach: Remote accessibility ensures trials include participants from diverse backgrounds.
Compliance: Automated documentation and tracking meet regulatory requirements effortlessly.
By bridging the gap between patient-centric care and cutting-edge logistics, Delve Health enables clinical trials to achieve both operational excellence and compassionate engagement.

Why Choose Delve Health?
With Delve Health, you gain access to a unique combination of expertise in eConsent and clinical trial IRT. Our commitment to simplifying clinical research while keeping patients at the center sets us apart. Whether you’re a researcher or a patient, our platforms make the trial experience seamless, reliable, and efficient.

Start Your eConsent & IRT Journey with Delve Health Today
Are you ready to redefine clinical trials with eConsent and IRT? Let Delve Health guide you through every step of the process with our innovative technology.

Address: 8100 Wayzata Blvd, Golden Valley, MN 55426, United States
Phone: +1 952-200-6228