Protocol Optimization & Site Selection

Verana Health's Protocol Optimization & Site Selection

Leverage Real-World Data for Faster, Smarter Clinical Trial Site Selection

Verana Health’s Site Explorer tool – powered by exclusive real-world data (RWD) from the American Academy of Ophthalmology (Academy) IRIS® Registry (Intelligent Research in Sight) and the American Urological Association (AUA) Quality (AQUA)® Registry – provides life sciences companies and CROs with unparalleled access to some of the largest and most clinically rich datasets in ophthalmology and urology. By leveraging this high-quality RWD, you can build effective study cohorts and select optimal trial sites in minutes. Site Explorer allows you to tap into a vast network of RWD to power your clinical trial site selection strategy, identify potential referral sources, and improve access to diverse patient populations.

~80M Patients in the IRIS Registry

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Verana Health is Reimagining Protocol Optimization and Site Selection

Powered by Exclusive Real-World Data

Verana Health has exclusive access to clinically rich EHR data from the Academy’s IRIS Registry, allowing you to tap into unique datasets and real-time insights, buried in EHRs, that you won’t find anywhere else.

Key Insights Into Potential Study Sites and Participants

Site Explorer provides detailed information on potential study sites, including practice-level trial experience, participant demographics, and site-specific clinical trial history at the indication level.

Regularly Updated, Comprehensive Data

The data is refreshed regularly, ensuring that your protocol optimization and clinical trail site selection decisions are always based on accurate and up-to-date data.

Key Benefits of Site Explorer

Build Cohorts and Identify Sites in Minutes

Quickly identify sites with a high volume of potential study participants that meet your trial's inclusion and exclusion (I/E) criteria.

View De-identified Patient Data at Scale

Access data on more than 80 million de-identified patients from 15,000 contributing clinicians in the IRIS Registry and 13 million de-identified patients from over 3,800 clinicians in the AQUA Registry.

Optimize Your Clinical Trial Site Selection Strategy

Combine clinical outcomes data, trial experience, and practice-level research contacts to ensure you select the right sites for your study.

Supporting Data for Clinical Trial Site Selection

Multiple Indications Supported

Site Explorer offers deep insights into trial experience across multiple indications. Learn more about our ophthalmology and urology indications.

Data Refreshes

Monthly data updates ensure you have access to the latest potential participant and site information.

Practice-Level Trial Experience

Understand a site’s previous clinical trial experience down to the indication level, and leverage these insights for faster and more accurate site selection.

Tailored Solutions for Sponsors and CROs

CROs

Engage with Sponsors: Highlight your data-driven approach to protocol optimization and site selection. Accelerate your ability to respond to RFPs and provide detailed estimates of practice and patient counts to enhance your proposals.

Adapt to Challenges: Respond quickly to trial challenges by exploring rescue strategies and leveraging RWD to make informed adjustments.

Unlock the Power of Real-World Data for Your Trials

With Verana Health’s Site Explorer, you can make smarter, faster decisions for protocol optimization and site selection. Contact us today to learn how our data-driven approach can accelerate your clinical trials.