Welcome to a new era in clinical research—where paper forms are replaced by smart tech, and trial participation becomes more accessible, engaging, and secure. At Delve Health, we're transforming the clinical trial landscape using eConsent software clinical trials, wearable monitoring devices, and automation tools like IRT (Interactive Response Technology).
Through digital innovation, we're making research more inclusive and efficient for sponsors, sites, and participants alike. Whether you're running a local pilot study or a global multi-site trial, our platform ensures you have everything you need to succeed. 🌐
🏢 About Delve Health
Delve Health is a forward-thinking health technology company driven by a mission to simplify and modernize the clinical trial process. We provide a comprehensive platform that integrates eConsent software for clinical trials, remote patient monitoring, IRT systems, and digital engagement tools.
With a global vision and a human-centric approach, we empower researchers and participants to connect more meaningfully, efficiently, and safely.
🎯 Our Mission
Our mission is to reimagine clinical trials through seamless technology that improves understanding, increases patient access, and boosts retention. By removing traditional barriers, we aim to make clinical research smarter, faster, and more inclusive.
We are committed to:
✅ Expanding access through remote participation
✅ Educating patients with interactive, multimedia eConsent
✅ Reducing trial costs with automation and digital workflows
✅ Supporting researchers with real-time insights and data
💡 What is eConsent Software in Clinical Trials?
eConsent software clinical trials replace outdated, paper-heavy consent forms with engaging, user-friendly digital experiences. Instead of overwhelming participants with paperwork, we provide interactive content—videos, visuals, and plain-language explanations—that help patients clearly understand the trial before signing. ✍️
Participants can review and sign informed consent documents remotely, using their smartphone, tablet, or computer—ensuring convenience, compliance, and clarity. 💻📜
🧩 Key Features of Our eConsent Platform
🎬 Interactive Multimedia Content
Participants view explainer videos, browse infographics, and interact with Q&A sections—making complex information easier to understand.
🖋️ Secure Digital Signatures
eConsent allows for legally valid, time-stamped electronic signatures that streamline onboarding while meeting regulatory requirements.
🔔 Real-Time Document Updates
Any protocol or consent form changes are instantly available to participants, ensuring transparency and up-to-date communication.
🔐 Compliance-First Framework
Every step in the consent process is logged automatically, creating a comprehensive audit trail ready for FDA, IRB, and global regulatory submissions.
⌚ Real-Time Monitoring with Wearable Tech
Delve Health incorporates wearable devices to monitor participants’ vital signs in real time—offering researchers continuous, accurate data without frequent clinic visits.
Wearables track:
❤️ Heart rate
💢 Blood pressure
🫁 Oxygen levels
🌡️ Body temperature
This data helps evaluate treatment safety and effectiveness while enhancing participant comfort and reducing the burden of travel.
🧠 Streamline Operations with Interactive Response Technology (IRT)
Our built-in IRT system automates critical study processes to ensure efficiency and precision. With Delve Health, you can:
🔁 Randomize participants automatically
💊 Manage drug supply across sites
📊 Access real-time trial data and metrics
📦 Track inventory and shipment logistics
IRT integrates seamlessly with our eConsent and wearable platforms—creating a full digital ecosystem for modern trials.
🌍 Global Access, Remote Participation
No matter where participants are located, our platform enables them to join, consent, and engage in trials remotely. This flexibility allows you to expand your reach, increase diversity, and speed up recruitment without geographic limitations. 🗺️💊
🌟 Benefits of Using eConsent Software Clinical Trials
✨ Faster Enrollment – Participants can sign up from anywhere in minutes.
📚 Better Understanding – Multimedia content makes consent more educational and less intimidating.
🔒 Higher Compliance – Built-in checks and digital logs help meet all regulatory standards.
📉 Lower Costs – Eliminate paper, postage, and redundant site visits.
🚀 Improved Retention – Engaged, informed participants are more likely to stay involved in the trial.
🤝 Why Choose Delve Health?
Choosing Delve Health means embracing smarter, more patient-friendly research solutions. Here's what sets us apart:
🔹 Expertise in eConsent software clinical trials, wearables, and IRT
🔹 Seamless integration with EDC, CTMS, and patient portals
🔹 Dedicated support for sponsors, CROs, and clinical sites
🔹 Scalable for studies of any size—from single-site to multinational
🔹 24/7 assistance and training for a smooth digital transition
We're here to make clinical trials faster, safer, and more participant-centric. 💬
🔧 Integrated, All-in-One Platform
Delve Health offers a unified clinical trial platform that combines:
📲 eConsent software
⌚ Wearable device integration
📦 IRT for operations
📡 Remote communication tools
This means fewer vendors, less complexity, and more control over your research.
✨ Let’s Build the Future of Clinical Trials Together
From protocol to patient, Delve Health delivers innovative solutions that simplify trial workflows, enhance patient experiences, and improve data accuracy. If you're ready to digitize your trials and connect with participants in smarter ways, we’re here to help.
Let’s reimagine research—together. 🌐📈
📍 Contact Us
📌 Address: 8100 Wayzata Blvd, Golden Valley, MN 55426, United States
📞 Phone: +1 952-200-6228
🌐 Website: https://delvehealth.com
Stay Connected
👍 Facebook: https://facebook.com/delvehealth
🐦 Twitter: https://twitter.com/DelveHealth
🔗 LinkedIn: https://linkedin.com/company/delve-health
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