Verana Health’s exclusive real-world data network and clinically true Qdata™ can help accelerate clinical trials in ophthalmology, urology, and neurology—from study startup through recruitment.
From protocol development and clinical trial design to site selection and identifying potential participants*, we help speed patient enrollment to help you meet your recruitment goals. Find out how Verana Health can support your next rare disease, site-based, or multi-disciplinary study.
Utilize Verana Health’s exclusive Qdata to help refine your protocol design and patient cohort, including both patient and site feasibility analyses. Qdata is derived from exclusive speciality electronic health records (EHRs), so we can help you better understand whether a site will have patients who fit study criteria in near real-time. We can help you refine the inclusion and exclusion criteria to best meet your enrollment and study goals.
Leverage Verana Health’s exclusive Qdata to not just identify, but also engage, clinical trial sites for your upcoming or ongoing study. Qdata contains variables that are key to site selection including: number of providers per practice, counts of complex procedures, generalized, de-identified patient demographics, and previous trial participation history. We can help you optimize for sites with trial experience and high patient volume in your indication of interest.
Utilize Qdata to help locate practices with providers serving patients who fit your protocol inclusion and exclusion criteria. We will create a unique algorithm to apply to Qdata for your specific trial using both structured fields and unstructured physician notes to identify potentially eligible patients. Verana Health will then support site activation for eligible sites and activate Verana Health Trial Connect to identify potentially eligible patients to the providers and research staff treating those patients. Verana can help sponsors stay on top of the patient recruitment progress through our operational metrics and updates and leave the site support to Verana Health’s team.
Verana Health can help practices treating patients with rare conditions match those patients to relevant trials, and if eligible, offer them no-cost genetic testing and counseling.
Verana Health can help practices identify and treat patients who match study inclusion and exclusion criteria, and to refer them to investigators at existing trial sites.
Verana Health collaborates with Clinical Development teams across the drug or device lifecycle from phase one to four of the clinical program. We leverage real-world insights to help support your protocol development, clinical trial design, site feasibility and analysis, and can help identify potential participants for your study.
Verana Health works with Clinical Operations professionals to help them by aiding in trial design, site selection, site onboarding, and patient recruitment to accelerate trial delivery. We support teams as they design, plan and physically run trials using real-world evidence.
Verana Health collaborates with Contract Research Organizations (CROs) to accelerate study recruitment through site identification and patient enrollment leveraging tools such as Verana Trial Connect.
One of Verana Health’s clients was looking to understand the ideal profile of patients who would fit their study criteria including their demographics, clinical characteristics, treatment patterns and outcomes. The client worked with Verana Health to leverage our de-identified Qdata that was generated from structured fields and physician EHR notes.
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One of Verana Health’s clients sought to develop therapies for unique manifestations of certain diseases. Verana Health helped the client leverage de-identified Qdata to identify specialty sites that may co-manage patients with these particular diseases, enabling the client to identify the most appropriate sites for their clinical trial.
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One of Verana Health’s clients was looking to find patients with a rare, inherited disease for their gene therapy clinical trial. They worked with Verana Health to leverage de-identified Qdata to help locate practices serving populations who fit the study criteria. Verana Health then conducted site outreach and worked with sites to ensure that potentially eligible patients were known to the clinical researchers. Practices then referred patients for genetic testing at no cost to the patients. Patients who were a fit for the trial were then referred to a study site.
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Life Sciences Companies are Customers
Providers Participate in our RWD Network
De-identified Patients Included in our RWD Network
Peer-reviewed Studies Published Using Verana Health Data
Therapeutic Areas with Numerous Diseases
Years Longitudinal Data
We partner with the American Academy of Ophthalmology and manage its IRIS® Registry (Intelligent Research in Sight) with more than 17,000 participating providers.
We partner with the American Urological Association and manage its AQUA Registry with more than 2,100 participating providers.
We partner with the American Academy of Neurology and manage its Axon Registry® with more than 1,400 participating providers.
Exclusive real-world data network of more than 20,000 healthcare providers in ophthalmology, urology, and neurology.
Clinician-directed and AI-enhanced population health data engine powering an advanced data integrity feedback loop.
Research-ready, disease-specific data modules to power quality insights for real-world evidence and clinical trial activation.
Advanced, clinically driven Artificial Intelligence techniques infused throughout the data process across both structured and unstructured data.
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*Verana Health provides principal investigators a HITRUST certified, HIPAA compliant portal to help them securely and privately identify their own patients who met eligibility criteria for the trial.
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