Delvehealth

1. ? Transforming Clinical Trials with eConsent & Wearable Tech ?? Welcome to the future of clinical trials, where convenience, innovation, and patient empowerment come together. At Delve Health, we are leading the charge by revolutionizing research with clinical trial eConsent, wearable vital sign monitors, and cutting-edge IRT (Interactive Response Technology). With digital-first solutions, we’re eliminating barriers and making clinical trials more accessible, efficient, and accurate—for both researchers and participants. Whether you're a sponsor looking to streamline your study or a patient curious about joining a trial, Delve Health brings a smarter way to engage. ? ? About Delve Health Delve Health is a technology-driven leader in the clinical research industry. We specialize in digital solutions that make trials simpler, smarter, and more patient-friendly. Our core mission is to improve clinical trial experiences through innovation, offering tools like clinical trial eConsent, wearable monitoring devices, and centralized platforms for real-time communication and data management.

2. From startup studies to global research projects, we are helping to transform healthcare—one trial at a time. ? ? Our Mission Our mission is to empower both researchers and patients by creating inclusive, tech-enabled trial experiences. By using digital tools like eConsent, we’re replacing outdated paperwork with intuitive, user-friendly interfaces that inform and engage. We aim to: ● Increase patient access through remote enrollment ? ● Ensure transparency with interactive consent forms ? ● Improve trial compliance through automated tracking ? ● Enable real-time insights using wearable health tech ? We’re building a world where clinical trials are faster, more inclusive, and powered by data—not paper. ??

3. ? What is Clinical Trial eConsent? Clinical trial eConsent is a digital alternative to traditional paper-based informed consent. Using visual tools, videos, and interactive content, it provides participants with a better understanding of the study they're joining. Instead of signing stacks of documents, participants can review study details on their devices and sign electronically—ensuring clarity, convenience, and compliance. ✍? ? Key Features of Our eConsent Platform ? Visual & Interactive Elements Participants watch videos, explore infographics, and read clearly written content to understand risks, benefits, and expectations. ? Legally Valid Digital Signatures Secure, trackable electronic signatures streamline the consent process while ensuring full regulatory compliance. ? Real-Time Updates Instant access to protocol changes and updated consent documents helps keep participants informed. ? Built-In Compliance Tools Every interaction is logged automatically, providing a complete audit trail for FDA and IRB submissions.

4. ? Real-Time Health Monitoring with Wearables We integrate wearable vital sign monitors into our clinical research platform to gather real-time data on participants’ health. These devices track: ● Heart rate ❤ ● Blood pressure ? ● Oxygen saturation ? ● Body temperature ? By capturing this data continuously, researchers can better assess treatment safety, efficacy, and participant wellbeing—without requiring constant in-person visits.

5. ⚙ Clinical Trial IRT: Smarter Trial Management IRT (Interactive Response Technology) automates critical trial functions, such as: ● Participant randomization ? ● Drug supply management ? ● Real-time reporting ? When combined with eConsent and wearable devices, IRT makes clinical operations seamless and data-rich. ?? ? Global Accessibility & Remote Participation With our platform, participants can join clinical trials from anywhere—home, work, or while traveling. No need to visit a clinic for every update or assessment. This remote model increases diversity, breaks down geographic barriers, and gives more people access to promising treatments. ?? ? Benefits of Using eConsent in Clinical Trials ✅Faster Enrollment: Patients can review and sign forms remotely, reducing onboarding time. ✅Improved Understanding: Visual content helps participants grasp complex information. ✅Fewer Dropouts: When patients understand their role and responsibilities, they’re more likely to complete the trial. ✅Better Compliance: Automated logs and alerts help maintain regulatory standards. ✅Cost-Efficiency: Digital processes save time and reduce paper and printing expenses. ? Why Choose Delve Health? At Delve Health, we blend technology with compassion to create clinical research tools that work for everyone. From trial design to patient engagement, we’ve created an ecosystem that is smart, efficient, and easy to use. Here’s why researchers and sponsors trust us: ● Years of expertise in clinical trial eConsent, IRT, and wearables ?

6. ● Seamless platform integration with EDC, CTMS, and other tools ? ● 24/7 support and training for sponsors, sites, and participants ? ● Scalable solutions for local and global studies ? ? Ready to Embrace the Future of Research? Whether you’re designing your first study or managing a multi-site global trial, Delve Health has the tools to make your project a success. From clinical trial eConsent to wearable monitoring and IRT automation, we deliver innovation where it matters most—at the intersection of science and human connection. ? Contact Us ? Address: 8100 Wayzata Blvd, Golden Valley, MN 55426, United States ? Phone: +1 952-200-6228 ? Website: https://delvehealth.com Stay Connected: ? Facebook: facebook.com/delvehealth ? Twitter: twitter.com/DelveHealth ? LinkedIn: linkedin.com/company/delve-health