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Regulatory Grade Oncology RWD

At COTA, we are revolutionizing healthcare by leveraging advanced data analytics to provide accurate and patient-centered insights. Our innovative approach is transforming the way healthcare is delivered, improving outcomes and reducing costs.

The COTA Difference:

  • Our standard datasets include more elements than
    our competitors
  • COTA’s depth of data is unmatched
  • 50/50 mix of academic and community data sources
  • Tech supported human abstraction creates the highest quality and most complete RWD
  • Led by oncologists who inform our curation methodologies
  • 1 of 2 oncology RWD companies with regulatory grade data
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Consent(Required)

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Why Use
Real-World Data?

At COTA, we curate regulatory-grade oncology RWD with the most relevance for our life sciences and provider partners, whether that involves supporting regulatory filings or research questions. We cannot unlock the full value of RWD without the highest-quality collection and curation methodology, and we are powering a revolution in the development of new cancer therapies to bring clarity to cancer care.

Provenance

COTA manages the entire lifecycle of data, from the initial abstraction of raw data to the final delivery of curated real-world data (RWD). We ensure complete traceability of our data, detailing its origins, the transformations it undergoes, and the quality assurance checks it passes through. Additionally, our process supports full auditability by regulators and other stakeholders, maintaining transparency and accountability at every step.

Relevance

Our process accurately identifies the appropriate cohorts by applying specific inclusion and exclusion criteria to ensure the right volumes. This approach guarantees representativeness across both real-world and clinical trial populations. Additionally, our coverage spans across various geographies of interest, ensuring comprehensive data collection and relevance in diverse settings.

Fidelity

Our methodology ensures a faithful representation of the original clinical data documented in electronic health records (EHR). We utilize technology-enhanced human abstraction to accurately understand and capture clinical nuances. The accuracy of our data capture is further guaranteed by a documented, multi-step quality assurance and quality control (QA/QC) process.

 

We have a responsibility to drive the use of RWD by consistently improving our data and demonstrating its utility. Our data has been used to support FDA and EMA submissions, explain care patterns, understand patient outcomes, and much more – and we anticipate the number of use cases to multiply in the coming years as RWD is explored and leveraged by more and more innovators in the industry.

 

Interested in learning more about how we can transform cancer care together?