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Instant health data for clinical trials eligibility

Quickly and easily include or exclude participants at every stage of your unique clinical trial.

Irix® makes life easier in life sciences. This groundbreaking SaaS tool helps determine a participant’s eligibility in real time at each critical milestone in your clinical trial—from pre-screening through enrollment and ongoing evaluation.

Irix empowers you to enroll the right participants faster, reduce site burden, flag adverse events and protocol deviations, and ensure your trial’s integrity.

With basic participant information and a HIPAA authorization, Milliman IntelliScript can instantly return years of interpreted, structured prescription histories and medical claims data on nearly any U.S. individual.

There’s no need to sift through error-prone questionnaires and interview notes for trial recruitment or rely on participants to monitor changes that threaten their continued eligibility. Instead, we configure our fully automated Irix Rules Engine to spot your trial’s inclusion and exclusion criteria in a wealth of health data. The Rules Engine interprets each participant’s Prescription Data and Medical Data to determine eligibility—so you can identify qualified participants or confirm continued eligibility in seconds.

Recruiters, sites, CROs, and sponsors are using this secure, thoroughly operationalized, and game-changing technology.

  • Accurate, individually identifiable health data
  • Rules engine automatically highlights trial eligibility, protocol deviations, and adverse events
  • Results within seconds

See better clinical trial results across the board with structured, interpreted health data.

Stop relying on participants’ memories, digging through notes, or running unnecessary labs. Our unique SaaS solution is affordable, accurate, secure, and backed by great customer service.  Talk to us about piloting Irix to help you:

  • Identify the best trial participants
  • Prevent ineligible subjects from randomizing
  • Flag protocol deviations
  • Minimize adverse events
  • Reduce site burden and costs
  • Bring more trials to completion

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    Let's make life easier in life sciences.

    Eligibility ... automatically. Learn how Irix can help you enroll the right participants faster, reduce site burden, flag adverse events and protocol deviations, and ensure your clinical trial’s integrity.