OVERVIEW
Tailored solutions for biotech companies
We understand the unique challenges that emerging biotech companies face – from navigating complex regulatory pathways to managing tight budgets and accelerated development timelines.
That’s why our comprehensive, cost-effective, and customized single-partner solution helps your clinical trials generate high-quality data with speed, efficiency, and scientific precision.
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 –
Regardless of trial size or complexity
Unlock the full potential of your clinical trials with our unparalleled expertise, cutting-edge endpoint solutions, and dedicated support that streamline your path to approval and accelerate your biotech innovation journey.
Scientific and regulatory expertise
With decades of experience and a dedicated team of over 140 scientific and medical experts, We provide biotechs with industry-leading support in trial design, endpoint selection, and regulatory compliance. Our teams will support you throughout the study lifecycle to meet critical milestones with streamlined setup and real-time access to your trial data and insights.
We will help ensure your studies adhere to evolving regulatory requirements, de-risking your development journey and optimizing your path to approval while reducing the need for costly internal scientific medical teams or high-cost external KOL consultants.
Click on one of the solution areas below to see the related team.
Comprehensive endpoint solutions
We deliver integrated efficacy, safety, and quality of life assessments across all therapeutic areas, with solutions optimized for all phases of development.
Whether you require Imaging, eCOA/ePRO, Cardiac, Respiratory or Movement endpoints, our solutions drive reliable, high-quality data to support decision-making and regulatory submissions.
Concierge-level support
Biotech companies need agile, scalable operational support to keep trials on track, and we deliver with responsive, high-quality global teams that adapt to your study milestones.
Our specialized project management teams are trained to meet the unique needs of biotech organizations, so you can have seamless execution and proactive risk mitigation. But we go beyond providing solutions – we guide you every step of the way.
As your strategic partner, we offer hands-on support from protocol development to regulatory submissions and trial execution, acting as an extension of your organization to deliver 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 biotech 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 endpoint solutions for early safety and efficacy insights
- Regulatory strategy support
Late-phase and pivotal studies
- Scalable endpoint solutions to meet growing data demands
- Advanced analytics for real-time decision-making
Regulatory and market access support
- High-quality data to enable submission success
- Meaningful insights to support reimbursement strategies
- Quality-of-life assessments to demonstrate treatment impact
Unlock the full potential of your clinical trials with Clario
Partner with us to accelerate your biotech innovation. Our proven expertise, cutting-edge technology, and tailored approach empower you to bring life-changing therapies to market with confidence.
Ready to optimize your trial? Contact us today to learn more about how we can support your next clinical trial.