OVERVIEW
Driving efficiency, engagement, and scientific excellence
Global pharmaceutical companies manage some of the industry’s most complex, high-stakes clinical trials. Clario delivers a single-partner solution that seamlessly integrates scientific expertise, innovative technology and operational excellence – empowering you to accelerate development, minimize risk, and bring transformative therapies to market with confidence.
50+
years of experience
30,000+
clinical trials
700+
FDA and EMA new drug approvals
100+
countries
70%
of all FDA approvals between 2012-2025
24/7
customer and patient support
SOLUTIONS AND EXPERTISE
At Clario, we simplify the difficult
We stand as a strategic partner in clinical trials, offering unmatched scientific and regulatory expertise, comprehensive endpoint solutions, and concierge-level support across all phases of drug development.
Scientific and regulatory expertise
With decades of experience and a dedicated team of over 140 scientific and medical experts, We help optimize endpoint strategy providing industry-leading support in trial design, endpoint selection, and regulatory compliance. Our teams ensure your studies adhere to evolving global regulations, de-risking your development journey and optimizing your path to approval.
Click on one of the solution areas below to see the related team.
Comprehensive endpoint solutions
We deliver efficacy, safety, and quality of life assessments across all therapeutic areas and trial phases, for seamless continuity throughout your drug development lifecycle from PI through to regulatory submission and beyond.
Whether you require Imaging, eCOA, Cardiac, or Respiratory endpoints, our solutions drive reliable, regulatory-grade data to support decision-making and regulatory submissions.
Scalable, high-volume trial management
With an expansive global footprint, we deliver the agility and scale required for today’s most demanding clinical trials.
Our expert teams seamlessly coordinate multi-continent operations, manage vast patient populations, and optimize high-volume data collection – so your trial progresses on time and on budget.
Concierge-level support for global pharma
We don’t just provide solutions – we guide you every step of the way.
With Clario, you gain a strategic partner that offers hands-on support, from protocol development to regulatory submissions and trial execution. Our expert teams act as an extension of your organization, ensuring you receive white-glove service tailored to your specific study needs.
Broad therapeutic area expertise
We support clinical trials across a wide range of therapeutic areas, so that no matter your indication or trial design, you have access to tailored endpoint solutions. Our deep experience spans neurology, oncology, cardiovascular diseases, metabolic disorders, respiratory, and more – helping pharmaceutical sponsors generate high-quality data to meet regulatory expectations.
Supporting your success at every stage of development
Preclinical and early-phase trials
- Scientific consultation to optimize trial design
- Digital endpoints to streamline data collection
- Regulatory strategy support
Late-phase and pivotal studies
- Scalable endpoint solutions to meet growing data demands
- Advanced analytics for real-time decision-making
- AI-driven patient engagement and retention strategies
Regulatory and market access support
- Regulatory-grade data for submission success
- Insights to support reimbursement and payer strategies
- Quality-of-life assessments to demonstrate treatment impact
Let’s transform your clinical trial success
Connect with Clario’s experts today to see how we can accelerate your next breakthrough.