Technology adoption for non-tech sites: bridging the gap in digital trials
Not every site is digital-ready, but your technology should be As clinical trials become more complex and regulated, the expectation for digital adoption grows. Tools like eCRD, CTMS, and ePRO are no longer optional, they’re essential. But while the industry pushes for standardisation, not every site is equally prepared for
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When to start using digital tools in your clinical trial timeline
ePRO in long-term trials: designing for patient fatigue
Why small sites need a CTMs too
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Technology adoption for non-tech sites: bridging the gap in digital trials
Not every site is digital-ready, but your technology should be As clinical trials become more complex and regulated, the expectation for digital adoption grows. Tools like eCRD, CTMS, and ePRO are no longer optional, they’re essential. But while the industry pushes for standardisation, not every site is equally prepared for this shift. Smaller or less tech-experienced research sites often struggle
When to start using digital tools in your clinical trial timeline
Adopting digital tools in clinical research is no longer a question of if, but when. From site start-up to data collection and monitoring, systems like eCRD, CTMS, ePRO, and eTMF help streamline operations, improve compliance, and reduce administrative burden. But how early should these systems be introduced into your study timeline? At Xolomon, we often hear this question from sponsors,
ePRO in long-term trials: designing for patient fatigue
When it comes to long-term clinical trials, patient engagement is everything. But as time goes on, even the most committed participants can lose motivation, especially if the burden of reporting becomes repetitive or intrusive. That’s where a well-designed ePRO (electronic Patient-Reported Outcome) system makes all the difference. At Xolomon, we believe digital tools should support, not overwhelm, patients throughout the
How to avoid mistakes when using eTMFs
Adopting an electronic Trial Master File (eTMF) is a key step towards more efficient, compliant clinical trials. But moving from paper to digital isn’t as simple as uploading files and forgetting about them. An eTMF is a living system, one that must be actively managed to ensure it delivers on its promise. In this article, we explore some of the
