OVERVIEW
Elevate your clinical trial success
In today’s competitive clinical research landscape, CROs need trusted partners who enhance their capabilities, streamline operations, and ensure the highest quality data. Clario offers partnerships with CROs of all sizes to strengthen your service offerings, helping you win more business and deliver successful trials with speed and precision.
50+
years of experience
26,000+
clinical trials
700+
FDA and EMA new drug approvals
100+
countries
60%
of all FDA approvals between 2012-2023
24/7
customer and patient support
SOLUTIONS AND EXPERTISE
At Clario, we simplify the difficult –
Enhance your trial offerings with comprehensive endpoint solutions
CROs partnering with Clario gain access to a full suite of integrated efficacy, safety, and quality-of-life assessments across all therapeutic areas and trial designs. Our expertise in Imaging, eCOA, Cardiac, or Respiratory endpoints enables the delivery of high-quality, regulatory-grade data that enhances trial outcomes and supports seamless regulatory submissions.
Deep scientific and regulatory expertise
Early scientific engagement is key.
With a dedicated team of over 140 scientific and medical experts, Clario provides unmatched support in endpoint selection, study design, and regulatory compliance. Our expertise helps CROs navigate evolving global regulations, optimize their sponsors’ endpoint strategy, and help trials remain on track for approval.
Click on one of the solution areas below to see the related team.
Drive efficiency and operational excellence
Clario’s global operational teams provide responsive, scalable support, allowing CROs to optimize workflows, reduce trial complexity, and accelerate study timelines. Our advanced technology platform seamlessly integrates with CRO systems, ensuring smooth collaboration, efficient data management, and streamlined trial execution.
A competitive advantage for CROs
By integrating Clario’s endpoint solutions into their service offerings, CROs can differentiate themselves in the market, enhance their credibility with sponsors, and secure more trial opportunities. Our commitment to data integrity, scientific excellence, and patient-centric solutions makes Clario the ideal partner for all CROs looking to deliver best-in-class clinical trials.
Vast therapeutic area expertise
CROs gain a competitive edge by partnering with Clario’s unparalleled therapeutic expertise spanning neurology, oncology, cardiovascular, metabolic disorders, respiratory, and more. Our broad experience ensures that no matter the indication, your trial benefits from tailored, scientifically rigorous endpoint solutions that meet regulatory expectations.
Providing seamless support across all trial phases
Study design and startup
- Expert consultation on endpoint selection and trial strategy
- Rapid study startup with proven processes and technology integration
- Regulatory insights to streamline approvals
Trial execution and monitoring
- Scalable, high-quality data collection and analysis
- Advanced analytics for real-time decision-making
- Seamless collaboration through integrated technology platforms
Regulatory and market access support
- Regulatory-grade data to support successful submissions
- Insights to enhance payer and reimbursement strategies
- Patient-centric outcomes to demonstrate real-world impact
Partner with Clario to maximize your impact
With Clario as your trusted endpoint solutions partner, your CRO can drive operational efficiency, deliver high-quality data, and enhance your competitive position in the industry.
Ready to strengthen your trial capabilities?