New, cutting edge technology designed for Patient Safety Data.
Peyra is the end-to-end solution for managing patient safety data. Peyra’s solution extracts, synthesizes, and validates Adverse Events and Concomitant Medications through direct integrations with existing systems. Peyra spot checks all the safety data before submission to ensure protocol adherence and avoid future queries. Beyond that, Peyra goes above and beyond by collaborating with sites to build customized, last mile tools, ensuring that existing workflows and preferences are respected, and that our technology adapts to your site, not the other way around.
Clinical trial operations have grown exponentially more complex over the past few years. The roles of Research Coordinators and Research Nurses include more responsibilities to squeeze in the same amount of hours in the day. This problem is evident with Adverse Events and ConMeds. Longitudinal views of the patient are required for making accurate attributions, but the existing tools aren’t set up to serve data this way. Instead, research staff are fishing for the correct data, with most submissions being rushed and resulting in sponsor queries.
Technology was meant to aid staff, but instead has added to the overhead, in large part due to systems not scaling to meet needs. New functionality was needed years ago, as was the need for the systems to communicate with each other. Research staff are now left with too many tools and too many manual workflows to do their jobs.
Patient safety data is time consuming to extract and nuanced to handle. Peyra believes this is the perfect place for technology to ease the burden on staff.
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Customized by Study
Peyra refers to study protocols to cross check Adverse Events, Grading, and reporting nuances.
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Proactive vs Reactive
Chasing down details is par for the course for research staff, and we know how delays of even a few days affect how much people remember. Peyra generates actionable steps for research staff so they can work on getting answers faster.
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Quality checks
Mistakes happen. Whether it's typos, conflicting information in a patient chart, or a missing date, Peyra catches these issues before they make it to the sponsor. Fewer queries make everyone happier.
Building easy to use solutions for research staff.
Coordinators currently track ConMed–AE relationships manually, across disconnected systems. Peyra automatically surfaces potential relationships, flags them for review, and prepares documentation — with the coordinator confirming every step.
Missed ConMed–AE relationships are among the most common sources of protocol deviations and safety reporting failures. This is one of the highest-stakes workflows in trial operations, and one of the most manual. Peyra changes that without removing the human from the loop.
