Overall compliance
92.0%
+5.2% vs goal
Diary completion (90 days)
95.0%
2–3× vs baseline
Compliance & retention for modern trials
Where Compliance Actually Happens
Delve Health blends eCOA, human concierge, and digital measures so your trials hit compliance and retention targets without adding burden for sites.
92–98% diary completion · 2–3× retention uplift.
Overall compliance
92.0%
+5.2% vs goal
Diary completion (90 days)
95.0%
2–3× vs baseline
Compliance & retention for modern trials
Where Compliance Actually Happens
Delve Health blends eCOA, human concierge, and digital measures so your trials hit compliance and retention targets without adding burden for sites.
92–98% diary completion · 2–3× retention uplift.
Delve Concierge
Online · 65+ languages
Outcomes that matter
Retention & compliance at scale.
Reduce dropouts with proactive, human-led follow-up and real-time alerts.
Increase compliance with multilingual support and personalized patient journeys.
Run hybrid and decentralized trials without adding vendors or complexity.
Access real-time data and analytics to make faster, better-informed decisions.
Patient Retention Over Time
Delve Health vs. industry average
Outcomes that matter
Retention & compliance at scale.
Reduce dropouts with proactive, human-led follow-up and real-time alerts.
Increase compliance with multilingual support and personalized patient journeys.
Run hybrid and decentralized trials without adding vendors or complexity.
Access real-time data and analytics to make faster, better-informed decisions.
Patient Retention Over Time
Delve Health vs. industry average
Trusted by leading pharma, biotech, and medtech teams
90–98%
eDiary / ePRO Completion
2–3×
Improvement in Retention
60%
Fewer Missed Tasks & Syncs
30%
Less Site Burden
Human-driven clinical trial
Concierge-as-a-Service™
Technology can remind. Humans get results. Delve’s concierges watch study activity in real time and step in the moment a participant drifts—protecting compliance before it becomes a deviation or a dropout.
They also pre-screen referrals, guide patients through structured questions, confirm interest, and deliver only qualified candidates to sites.
The result: higher completion, fewer dropouts, and calmer, more predictable studies.
Proactive Compliance
Real-time monitoring with fast, human follow-up.
Pre-screening
Calling referrals and qualifying only eligible, interested patients.
Multilingual Support
Empathetic outreach in 65+ languages.
Site Relief
We handle reminders, rescheduling, and participant questions.
One Platform. Four Pillars.
Delve wraps compliance and retention around an integrated digital platform—combining
eCOA, digital measures, consent, and analytics with a human layer that keeps
everything moving.
eCOA & ePRO
Accessible, multilingual diaries and outcomes that patients can actually complete.
Digital Measures
Validated, fit-for-purpose measures from wearables and sensors, ready for regulators.
Concierge-as-a-Service™
Human teams who own the work of keeping participants active, informed, and on schedule.
Compliance Analytics
Real-time dashboards that surface risk early and prove the health of your trial.
Who We Serve
Whether you’re developing a drug, launching a device, or leading a site network, Delve
Health surrounds your study with the compliance and retention support it needs
to finish strong.
Pharma
Protect pivotal endpoints with high diary completion and retention.
MedTech
Support post-market and real-world studies with engaged participants.
Biotech
Give lean teams an experienced compliance partner from day one.
Research Sites
Offload reminders, calls, and rescheduling so staff can focus on care.
The Difference Sites Feel Immediately
Before Delve
- Too many patient calls and reminders consuming coordinator time
- Manual prescreening lists draining staff capacity
- Device setup and troubleshooting taking hours
- Missed visits and last-minute rescheduling chaos
- Keeping multiple systems in sync by hand
- High turnover risk from coordinator burnout
With Delve
- Too many patient calls and reminders consuming coordinator time
- Prescreening assistance with escalation only when needed
- Clear device workflows + rapid troubleshooting for participants
- Visit confirmations and real-time coordination to prevent misses
- Cleaner handoffs across systems with fewer manual touches
- Reduced admin burden so coordinators focus on patient care
Sites reclaim hours every week — and patients stay supported between visits.
Proven in Global Studies
Post-Market Respiratory Study
Visits reduced 12 → 2. Diary completion > 95%. Retention: 94%.
Hybrid Oncology Program
63% increase in retention after layering in concierge support.
Digital Endpoint Enablement
35% increase in usable data within the first 14 days.
Testimonials
Trusted by clinical operations leaders.
Director of Clinical Operations, Global Biotech Sponsor
With Delve, we finally had one place to see compliance, retention, and risk. We completed enrollment three months early with cleaner data at database lock.
James Chen
VP, Clinical Development, Mid-size Pharma
One vendor instead of five simplified our operations dramatically. The concierge services alone were worth the investment.
Maria Rodriguez
Clinical Trial Manager, Leading CRO
Ready to Make Compliance Your Advantage?
Bring Delve into your next protocol as the compliance and retention layer so your team can focus on the science, not the chasing.