Product Overview
All the precision endpoint technology and services your virtual or hybrid trial needs to deliver more certain outcomes.
Clario advances decentralized clinical trials with the Power of Certainty
Decentralized clinical trials (DCT) continue to positively impact recruitment, retention and patient convenience, while expanding opportunities for diversity in clinical trials. Data integrity can still be preserved even when the responsibility for endpoint data collection moves from qualified staff to clinical study participants.
Clario’s scientific expertise, global scale and broad endpoint technology platform provide the certainty that clinical evidence in your DCT will be generated with reliability and precision.
Let us help you bring certainty to your decentralized clinical trial.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Endpoint and therapeutic area expertise reduce site and patient burden
- Simplify site and patient experiences for your decentralized clinical trials with Clario’s science-driven strategies.
- Deliver rich, regulatory-compliant data with support from Clario’s 200+ endpoint science and therapeutic area experts, who can advise on appropriate clinical outcome assessments for your hybrid or virtual trial.
Global coverage and local expertise in assessing drug quality and safety for all
- Scale your DCT globally and reach diverse and remote patient populations.
- Know that the right devices — properly configured — are sent to the right sites and patients thanks to Clario’s vast network of logistic hubs across Europe, Asia and the Americas.
- Evidence a product’s safety and efficacy with certainty by leveraging Clario’s worldwide capabilities — all backed by 50 years of global regulatory experience.
About the company
Experience
With 50 years of experience as a clinical trial data management company and 19,000 clinical trials, we have mastered the ability to collect the richest clinical evidence.
Reliability and precision
Through science-informed technology, we generate reliable and precise clinical evidence, regardless of trial location or evidence generating modality.
Proven global scale
Our global infrastructure has supported regulatory compliance in over 120 countries. With demand & inventory planning, device provisioning and logistics and 24/7 customer care, no one can scale the way we can.
