Training your team for eCRF success
Implementing an electronic Case Report Form (eCRF) system is a pivotal step in modernising clinical trial operations. But no matter how powerful your eCRF platform is, its success depends largely […]
Pharmacovigilance in clinical trials: how Xolomon supports safer, smarter studies
In clinical trials, patient safety isn’t just a regulatory checkbox; it’s the backbone of every protocol. Whether you’re running a single-site study or coordinating a multi-country trial, tracking adverse events […]
Tecnología al servicio de la investigación: el estudio Hemi-D-TREND confía en Xolomon
Nos enorgullece formar parte del reciente estudio Hemi-D-TREND, publicado en Surgical Endoscopy, que pone el foco en una pregunta clave: ¿cuál es el momento ideal para entrenar a cirujanos en […]
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 […]
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 […]
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 […]
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 […]
How digital tools reduce paperwork in clinical trials
Clinical trials generate a tremendous amount of documentation, from patient consent forms and visit logs to adverse event reports and regulatory submissions. Traditionally, all of this has been managed on […]
What should be in your first ePRO form?
When starting a clinical trial, patient data is everything. But how you collect that data can make or break the success of your study. Electronic Patient-Reported Outcomes (ePRO) have become […]
Why small sites need a CTMs too
There is a common misconception about clinical trial management systems (CTMS) that they are only useful for large sponsors or multinational studies. The reality is that smaller research sites often […]
