Case study
Clario supports accelerated FDA approval in non-small cell lung cancer study
Case study
Clario Supports Large Pharmaceutical Company with a Complex Alzheimer’s Disease Study
Case study
Keeping the participant in mind – an eCOA success story
Case study
Collaborative data management activities to prepare six years of data for submission
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Comprehensive Clinical Adjudication Solution Rescues a Study in Jeopardy
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Global biotech gains visibility into treatment-related risk of SIB
Case study
Training program reduces placebo effect by more than 50% in ePRO study
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High-quality compliant eCOA data captured across group of oncology studies
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Prospective Observational Study Benefits From BYOD* eCOA Solution
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Target my hives: a digital community bringing patients together
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Global pharmaceutical company drives data acceptability over 95%
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Observational study maximized enrollment through electronic data capture
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Simple effectiveness study deploys electronic data capture solution despite tight timelines
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Global pharmaceutical company proves efficacy of bronchodilator for COPD patients
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Vaccine developer achieves cost-effective and streamlined transition to electronic data capture
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Phase 4 study achieves greater patient engagement & improved data quality using electronic data capture
Case study
Merck research laboratories reduces standard deviation with electronic pro
Training and support
Our customer care teams provide comprehensive training programs and support services to sponsors, sites, patients and CROs, driving successful adoption and execution.
Targeted solutions for your therapeutic area
With over 200 therapeutic area experts, we deliver innovative, therapeutic area technology solutions and clinical trial data management systems to meet clinical trial objectives.
Expert operations to meet the standard of evidence you need
From project and clinical trial data management systems to customer care, manufacturing, and logistics, our expanding global operations team of over 1,700 employees has the expertise and capacity to scale to deliver the richest evidence — always.
Guiding you through every phase of regulatory approval
With our depth of experience in delivering clinical trials in over 120 countries, only Clario can help you with regulatory submissions for Phase 1-4 clinical trials and pre-and post-approval.