Clinical Trial Design
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.
Clinical Trial Site Section
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.
Patient Recruitment
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.
