Below you will find answers to some of the most frequently asked questions for EazyRI. We are continuously adding the most asked questions to this page, so if you have a question and don't see your answer, please don't hesitate to email us at [email protected].
Generic RIs are usually derived from small, Western cohorts and can misclassify up to 80 % of healthy patients in other regions; EazyRI tailors ranges to your population, reducing false positives/negatives and unnecessary followups.
With a simple CSV or Excel data upload, EazyRI applies its patent pending, IFCC/CLSIcompliant indirect algorithms to isolate healthy results and calculate new intervals—all fully automated.
No. The workflow is wizarddriven; results are delivered as ready to use PDF reports and, if desired, pushed back to your LIS with a single click (available on enterprise package).
Yes. Data stay in your jurisdiction, are pseudonymised on upload, and processed under GDPR/KVKK compliance. EazyRI never stores personally identifiable information, or your data.
EazyRI automatically recalculates reference intervals every time you upload or stream new results, ensuring that your ranges always reflect the latest patient population.
The statistical engine is aligned with CLSI EP28A3c and IFCC CRIDL recommendations and supports optional LAVE and partitioning rules for sex, age, and method differences (available in enterprise package).
Yes. We offer a 5 credit fully featured trial that lets you process up your data and preview your RI reports. You can contact us if your want to purchase more credits.