Prioritizing patient safety, reduced timelines, and high-quality data
Whether you are a biotech conducting your first Phase I study or a seasoned CRO performing post-market surveillance studies, our team of dedicated experts deliver credible, compliant, and high-quality data you can be certain of.
Our team has supported over 13,800 trials globally to:
- Improve patient safety and enrollment
- Increase data access leading to reduced timelines
- Deliver scientific-grade data to reduce variability
- Ensure devices are delivered on-time globally to avoid delays
Cardiac safety is the #1 reason for drug development failure and post-market recalls
Regardless of your therapeutic target, centralized analysis of your ECG and blood pressure data delivers highly precise results to ensure throughout understanding of the safety profile. This information, backed by our team of experts, helps you prioritize your pipeline and ensure regulatory compliance, saving you time and money.
Available solutions
Arrhythmia Analysis
Collect continuous ECG data with certainty in site-based or decentralized clinical trials with our flexible technology solutions and patient-friendly devices.
Blood Pressure Services
Collect and centrally analyze accurate, consistent, quality blood pressure data from site-based to decentralized trials.
ECG — On-site to DCT and Phase I-IV
Monitor every heartbeat with precision from anywhere to assess safety and efficacy throughout your site-based or decentralized clinical trial.
Phase I/TQT Cardiac Assessment
Fulfill your ICH E14 requirement early, minimize risk and potentially reduce costs throughout your trial by collaborating with our Phase 1 Center of Excellence.
Regulatory Consultation and Statistical Analysis Expertise
Leverage our industry key opinion leaders to understand the complex regulatory landscape while minimizing risk with confidence.
Cardiovascular Imaging
Global comprehensive centralized cardiovascular imaging services ensuring safe and effective treatments.
Advance your decentralized clinical trial with the power of certainty
Global capabilities
With Clario-operated logistics hubs in the US, EU and Japan with the largest, most diverse inventory of validated equipment and 136,000 devices shipped per year.
Clinical and scientific expertise
50 years of clinical trial experience in cardiac endpoints plus a team of cardiologists who bring more than 200 years of clinical expertise powers certainty.
The broadest endpoint technology platform
Our flexible equipment and overread services ensure consistent, quality data, so you can be certain you’re collecting credible data.
Patient-centric experiences
We help power trial continuity patient reminders, coaching and demonstrations to ensure patients experience success.
Proven results earn trust
13,887
trials supported
580
new drug approvals
50
years of science
600+
QT studies
200+
combined years of clinical experience
480+
unique programs
87+
approvals from TQTS alone
230+
sponsors
Cardiac Solutions Science Team
Increase confidence in site performance with Clario Certified Sites
Clario Certified Sites have completed our Certified Site program to ensure that each study is conducted in an optimal manner and results in the highest quality data. The certification program requires each site to go through an extensive training and testing process. These sites help sponsors reduce study start-up time with well-trained and well-equipped sites.
Related therapeutic areas
Learn more or speak with one of our experts
Our team of clinical trial cardiac safety experts are always available to address questions about our cardiac solutions. Submit your contact information and we’ll be in touch shortly.