CRO CLINICAL RESEARCH
Expand Your CRO Capacity With Speed and Precision
Meet tight deadlines with a Clinical Site that accelerates early-phase studies and strengthens your delivery to sponsors.
Delays Put Your Client Relationships at Risk
For CROs, every delay in clinical research studies risks more than just deadlines—it threatens sponsor confidence, contracts, and long-term partnerships.
You need a clinical site partner that expands your capacity and keeps trials moving without inflating costs to avoid.
- Missed Timelines — Slow enrollment jeopardizes milestones and sponsor expectations.
- Contract Risk — Delays in one study can impact multiple projects and client retention.
- Operational Burden — Teams spend more time troubleshooting than advancing research when studies stall.
Focused on Speed & Accuracy
Your Partner in clinical research providing high-enrolling clinical trial unit and Bioanalytical services for global CRO partners.
As a trusted clinical siten that has been conducting phase 1 trials for over 10 years and serving more than 150 global clients, Axis delivers early-phase studies designed to support CROs with:
- Pharmacology Studies — SAD / MAD, DDI, PK/PD
- First-in-Human (FIH) Studies
- Cardiac Safety Studies
- Dermatology Clinical Studies
- dOMF Studies
- ADME Studies
- Full Bioanalytical Lab Services
Keep Your Client Projects
On Schedule & Within Budget
Rapid Timelines
Fast start-up and enrollment at our dedicated clinical trial units.
Cost Efficiency
Smart processes and proven execution help CROs stay on budget.
Reliable Data
Submission-ready results you and regulators can trust.
Your sponsors expect speed, accuracy, and value. At Axis, we expand your capacity with high-enrolling clinical pharmacology units, integrated bioanalytical laboratory services, and expert staff who keep every project moving—without runaway costs.
A Clinical Research Center CROs Trust
Your Full-Service Clinical Trial Partner
Pharmacology Services
From SAD/MAD to DDI and PK/PD, our clinical pharmacology CRO unit delivers precision data to support your sponsors’ development timelines.
Dermatology Studies
From Irritation and adhesion studies to dermal PK/PD with dOFM technology,, Axis provides specialized methods and rapid recruitment.
hADME Studies
Generate critical pharmacokinetics ADME insights—absorption, distribution, metabolism, and excretion—with efficient study execution.
dOFM Studies
Dermal Open Flow Microperfusion studies deliver rich PK/PD data from fewer subjects, helping your clients advance confidently.
Early TQT Studies / Cardiac Safety
Conduct thorough QT studies with advanced ECG clinical trial monitoring and real-time cardiovascular safety data.
A Clinical Trial Unit Trusted
By Biotech Innovators
Built for CRO Speed
One of the largest U.S. clinical pharmacology units supporting CRO partners worldwide.
At the heart of Axis is our state-of-the-art clinical research center in Minnesota—one of the largest dedicated Phase I trial units in the U.S. Purpose-built for early-stage development, our site offers:
- 250+ Beds for healthy volunteer and patient studies.
- Integrated Bioanalytical Laboratory Services for faster turnaround.
- Experienced Clinical Research Specialists for precise, compliant execution.
Axis delivers the timelines, efficiency, and reliability CROs need to strengthen delivery to sponsors.
Why CROs Partner with Axis
CRO leaders choose Axis because we deliver speed, efficiency, and full-service clinical research support to keep projects moving.
Axis is a Clinical site with integrated bioanalytical solutions designed to help CROs deliver for their clients.
High-Enrolling US Site
Rapid start-up and large volunteer pools accelerate recruitment.
Cost Control
Efficient operations and proven processes keep budgets under control.
Regulatory-Ready Data
Reliable results aligned with FDA and global standards.
Complete Services
From pharmacology to bioanalytical services, everything is under one roof.
Don’t Let Delays Jeopardize Your Sponsor Deliverables
Partner with a clinical research organization that delivers speed, efficiency, and reliability—so your clients succeed.
What Our Clients Say
Real results and strong relationships—straight from the teams we’ve worked alongside.
"AXIS has consistently delivered outstanding support as a Phase 1 site partner. Their ability to recruit and enroll subjects quickly and efficiently has been a key factor in keeping our timelines on track. The team is professional, responsive, and well-organized, ensuring the smooth execution of even the most complex pharmacology studies. We value their expertise and look forward to continued collaboration."
"We've worked with AXIS Clinicals USA on several Phase 1 studies, and their ability to quickly enroll subjects has been a huge advantage for us. They’re efficient, easy to work with, and always meet our timelines. Their team handles everything smoothly, which makes our job easier. We’re grateful for their support and look forward to working with them again."
"Partnering with AXIS has been a transformative experience for us. Their team deeply understands the complexities of pharmacology cardiac safety TQT projects and has been exceptionally responsive and proactive at every stage. What could have been a challenging process was made significantly smoother, with seamless coordination between clinical and bioanalysis under one roof, keeping timelines on track and delivering high-quality data."
"AXIS has been our long-time reliable partner for clinical research. Their team understands the challenges of developing 505(b)(2) products and has provided solid support throughout our clinical development program of studies. They’ve helped us stay on track and navigate a complex process with professionalism and quality data. I would recommend them to all of my industry contacts looking for a dependable CRO partner."
Your Path to Fast
Your Roadmap to Fast, Reliable Phase 1 Clinical Trials
Every successful program depends on a clear plan. Here’s how Axis keeps your clinical trial on schedule, on budget, and designed to meet regulatory expectations.
Schedule a
Consultation
Share your client study details,
goals, and timelines.
Get a Custom Proposal
& Trial Timeline
Receive a proposal that's transparent, efficient,
and built to expand your capacity.
Deliver Results Fast with Confidence
Advance projects on schedule and strengthen sponsor trust.
Have questions or need expert support? Our team is here to help—reach out and let’s move forward together.
Get In Touch
Axis Blogs
Partner with a clinical research center that delivers fast timelines and reliable results.
- BLOG
How Novel Drug Delivery Systems Are Challenging Traditional BE Study Design
Bioequivalence (BE) studies have long relied on well-established assumptions about how drugs are administered, absorbed, and measured in the body.
- BLOG
How Genetic Variability Is Being Accounted for in Bioequivalence and PK/PD Studies
As drug development becomes increasingly global, sponsors are paying closer attention to how genetic variability
- BLOG
The Role of Metabolomics and Biomarker Analysis in Early Phase Clinical Trials
The rise of metabolomics and biomarker analysis in early phase clinical trials is reshaping how development teams evaluate pharmacological activity, human variability, and early indicators of safety.