Real-World Evidence Safety Studies

Harnessing Real-World Data for Post-Market Surveillance

Verana Health provides advanced real-world evidence Safety Studies solutions using Ophthalmology and Urology Qdata®—purpose-built, clinically rich datasets derived from the American Academy of Ophthalmology IRIS® Registry (Intelligent Research in Sight) and the American Urological Association (AUA) Quality (AQUA)® Registry.

Powered by our population health data engine, VeraQ®, these datasets are meticulously curated using advanced artificial intelligence and quality algorithms to transform vast amounts of raw healthcare data into a reliable understanding of real-world therapy performance. Our solution supports post-market safety surveillance, data for regulatory filings, and ongoing monitoring of treatment and product safety in real-world settings.

Use Cases for Real-World Evidence Safety Studies

  • Post-market surveillance: Conduct longitudinal safety monitoring of approved treatments and medical devices. Learn about one of our studies.
  • Risk assessment: Identify potential safety signals and assess adverse event patterns across diverse populations. Read a white paper.
  • Regulatory support: Generate evidence for regulatory filings and safety submissions, including FDA-required postmarketing studies. Read a case study.
  • Real-world risk management: Monitor ongoing product safety and support risk mitigation strategies. Read a case study.

Meet with the Verana Health Team or View a Demo

Why Choose Verana Health for Real-World Evidence Safety Studies?

With exclusive access to the IRIS Registry (ophthalmology) and the AQUA Registry (urology), Verana Health ensures robust and detailed real-world data insights. These registries allow for:

  • Large-scale data: Access to extensive EHR datasets from real-world clinical practices across the U.S.
  • Rich clinical detail: Detailed longitudinal data, including data from clinical notes that include treatment patterns, patient outcomes, and follow-ups, ensuring accurate safety signal detection.

Diverse patient populations: Comprehensive data that spans a broad demographic range from patients at academic medical centers, community practices, and more, ensuring that safety assessments are relevant across different patient subgroups.

Professional Services and Additional Data Linkage

Verana Health offers tailored insights projects, additional data linking, Data-as-a-Service (DaaS) capabilities to meet your unique study requirements:

  • Professional services: Our experienced team works closely with life sciences companies to customize real-world evidence safety studies and ensure compliance with regulatory requirements. From study design to data analysis and reporting, we offer full support at every stage.
  • Independent data linking: Leverage our advanced capabilities to link all Ophthalmology and Urology Qdata® with other datasets (e.g., claims data) to generate comprehensive safety profiles for the needs of life sciences companies.
  • Data-as-a-Service (DaaS): Access and analyze Qdata insights through our flexible, secure platform, tailored to support your research and data needs.
  • Intuitive dashboards: Utilize our Qdata Explorer application to explore expertly curated, disease-specific Qdata modules in ophthalmology. With its intuitive interface, Qdata Explorer can help your team quickly build and share patient cohorts, generate hypotheses, and run feasibility studies.

Why Partner with Verana Health?

  • Trusted Data: Our access to the IRIS Registry and the AQUA Registry — expansive ophthalmology and urology datasets in the U.S. — ensures comprehensive real-world data depth.
  • Advanced Curation: Our data science team applies advanced AI techniques, such as machine learning and natural language processing, with clinician oversight to generate real-world evidence from structured and unstructured EHR data.
  • Actionable Insights: By leveraging our research-ready data, you can gain actionable insights to inform product safety and make data-driven decisions.
  • Regulatory-Ready: Our data and analytics capabilities are designed to meet the rigorous requirements of regulatory bodies, ensuring seamless integration into your safety study needs.

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Contact us to learn more about Safety Studies solutions.