Fast Timelines & Clean Data with a Trusted Clinical Research Center
Accelerate your Phase 1 trial timeline with rapid recruitment, responsive experts, and a team that prioritizes your success.
You don’t have to choose between speed and quality. You can have both.
Many Pharma and Biotech companies are frustrated with the slow timelines and rigid processes when it comes to early phase trials.
In Phase 1 studies, time is a critical resource.
Fast, Reliable Data From
Experienced Clinical Research Specialists
We specialize in conducting high-quality early-phase and specialty clinical trials designed to deliver accurate results quickly.
- Pharmacology - SAD / MAD, DDI, PK/PD
- Cardiac safety
- Dermatology
- Dermal Open Flow Microperfusion
- ADME
Trusted Clinical Research Center
Quick Start-up
With optimized processes, have your first patients enrolled within weeks.
Rapid Recruitment
Access a large, engaged volunteer database to meet 100% enrollment target quickly.
Responsive Experts
Direct access to decision-makers who keep your trial moving.
Clean, Submission-Ready Data
High-quality, regulatory-compliant results delivered on time.
You’re in good hands from start to finish.
With a high-enrolling US Phase I site, experienced teams, and streamlined processes, AXIS Clinicals launches studies quickly and delivers clean, reliable data—helping you reach your next milestone on time with confidence.
A Clinical Trial Unit Trusted by Leading Innovators
Accelerating Discovery for Research Leaders
Biotech
Pharma
CRO
Your Clinical Research Center &
Partner From Day One
When you work with AXIS Clinicals, you get more than a CRO, you gain a dedicated partner who integrates seamlessly with your team.
From recruitment to data delivery, you get expertise, speed, and focus every step of your study.
Over the past 10 years, we have conducted over 300 early-phase studies specializing in
- Pharmacology
- Cardiac Safety
- Dermatology
- ADME
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 a Faster, Smoother Trial
It’s simple to get started and keep your study moving, so you can focus on your science, not roadblocks.
Schedule a
Consultation
Share your study details,
goals, and timeline.
Get a Custom Proposal
& Trial Timeline
Transparent, realistic, and built for
efficiency.
Advance to Phase II
Quickly with Confidence
Meet milestones on
schedule with reliable data.
Participate in a Study
Help Advance Medical Research
Join one of our clinical trials and play a vital role in bringing new treatments to patients.
Our studies are safe, carefully monitored, and led by experienced medical professionals.
Participation is compensated, and your contribution helps bring life-changing therapies closer to those who need them most.
Why Companies Partner with Axis
As a high-performing clinical research center, AXIS Clinicals offers integrated capabilities that combine speed, quality, and responsiveness to keep your trial on schedule and your goals within reach.
High-Enrolling US Site
Proven capacity to meet aggressive timelines.
Fast Recruitment
Submission-Ready Data
Milestone-Focused
Your Timeline Is Your Advantage
The faster you reach your milestones, the sooner you can advance your asset, secure funding, and continue your work.
As your trusted clinical research partners, Axis Clinicals delivers a team dedicated to keeping your trial on time and your momentum strong.
Experience faster trial timelines—
weeks, not months.
Don’t wait to get started!
Proven Success in Action
As a high-performing clinical research center, AXIS Clinicals offers integrated capabilities that combine speed, quality, and responsiveness to keep your trial on schedule and your goals within reach.
Free Guide:
5 Ways to Keep Your Phase I Trial on Schedule
A timely trial protects your milestones, budget, and momentum.
- Download our free guide and learn how to:
- Start faster without sacrificing quality
- Avoid common operational bottlenecks
- Keep your trial moving toward the next phase
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.