We hit your enrollment targets. We respond fast. We deliver quality data on time.
Patient enrollment is the single biggest bottleneck in clinical trials. Most sites overpromise and underdeliver. The fix is simple but not easy: quality sites that reliably enroll on target, on time.
Learn more about how we deliver below.
You need timely, truthful, and reliable feasibility in order to effectively design and execute your clinical trials. Denali delivers on all fronts.
<48 Hours
CDA/Feasibility
Completion
<48 Hours
for Contract/Budget
Responses
<21 Days
from Study Award to
Site Initiation
Our proprietary Denali Patient Recruitment Engine, which is supported by our 7-day-a-week in-house call center, delivers reliable enrollment even for the most challenging Pediatric studies.
<60 Days
to First Patient In
#1-3:
Our goal is to be in the top 3 sites globally for every trial we accept
92%+
retention rate
Through rigorous SOPs, continuous training, internal audits, and a culture of Kaizen, Denali is relentlessly dedicated to upholding the integrity and quality of trial data.
<48 Hours
Data Entry
<72 Hours
Protocol Amendment Implementation Time
<48 Hours
Query Resolution
Our exceptional team of clinical research professionals is what enables Denali to deliver exceptional results. We seek the best talent the industry has to offer and work on continuously cultivating and developing our team's strength.
<0.35%
applicant acceptance rate
One Efficient
Centralized Operating model
100%
training compliance rate
Ultimately, you need a responsive and reliable partner that does what they say they will do to support you in bringing your drug to market.
100%
on target enrollment*
24-48 Hours
response time
The sponsor was facing a six-month first-patient-in delay, with no sites activated nationwide and an urgent need to enroll 200 patients across 20 sites. With the study timeline at critical risk, the sponsor needed a site that could move quickly from activation to screening while still protecting data quality, eligibility standards, and participant readiness in a complex psychiatric trial.
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A complex diabetic wound healing study faced significant enrollment pressure across the site network. The protocol required specialized wound assessment capabilities, careful subject qualification, and long-term retention in a patient population that is often difficult to engage consistently. Many sites struggled to identify qualified subjects and keep them active through the study duration.
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