Clario
Science-informed endpoint technology and global clinical trial management for every phase of drug development.
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Clario provides comprehensive clinical trial endpoint solutions spanning cardiac safety, eCOA, medical imaging, respiratory, and precision motion analysis, supporting approximately 70% of FDA and EMA novel drug approvals over the past decade. Headquartered in Multiple (100+ countries).
Phases
Indications / Therapeutic Areas
Services
- Clinical Imaging Core Lab
- Data Management & eClinical
- Clinical Operations
- Phase I Clinical Trials
- Phase II Clinical Trials
- Phase III Clinical Trials
- Phase IV / Post-Marketing
- Biostatistics & Statistical Programming
- Regulatory Affairs
- Cardiovascular & Metabolic Specialty Services
- Central Laboratory Services
- Clinical Trial Services
- US FDA Regulatory Strategy
- EU EMA Regulatory Strategy
- Medical Writing
- CNS Specialty Services
Modalities
Technical specifications & accreditations
Accreditations
Infrastructure
About this organization
Overview
Clario is a leading provider of clinical trial endpoint data solutions serving pharmaceutical, biotech, and CRO customers across every phase of drug development. The company combines science-informed endpoint technology, global scale, and expert clinical trial management services to generate reliable clinical evidence.
Core Capabilities
Endpoint Technologies & Data Solutions:
- Cardiac safety monitoring and arrhythmia assessment
- eCOA (electronic Clinical Outcome Assessment) platforms including eCOA Live and eCOA Multimedia
- Medical imaging with clinical adjudication and AI-powered image redaction
- Respiratory endpoint solutions
- Precision motion analysis via the OPAL® System for movement disorders and neuroscience applications
- Trial enablement solutions including eConsent, source document management, eligibility assessment, and reporting analytics
Clinical Trial Management:
- Support for site-based, hybrid, and decentralized clinical trials
- 24/7 customer and patient support with integrated training and instructions
- Global deployment across over 100 countries with translations in over 100 languages
- Experience delivering over 30,000 clinical trials
Scientific & Regulatory Expertise:
- Team of hundreds of clinical trial management experts with therapeutic area and endpoint science specialization
- Extensive global regulatory experience supporting FDA and EMA submissions
- Clinical adjudication and statistical analysis capabilities
Scale & Impact
Clario's platform supports approximately 70% of FDA and EMA novel drug approvals over the past decade. The company operates globally with thousands of customer operations professionals and approximately 4,000 employees worldwide.
Locations
Global Operations
Multiple (100+ countries)
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