Simplifying administrative burden at research sites: How EDC can help
In clinical trials, quality data and regulatory compliance are non-negotiable. But for many research sites, the growing mountain of administrative tasks, from repetitive form-filling to data transcription and query resolution, is becoming a serious problem. Site staff are spending more time managing paperwork than caring for patients or advancing the
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How to prepare your team to work with an eCRD system
Ensuring data security in clinical trials: best practices
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Simplifying administrative burden at research sites: How EDC can help
In clinical trials, quality data and regulatory compliance are non-negotiable. But for many research sites, the growing mountain of administrative tasks, from repetitive form-filling to data transcription and query resolution, is becoming a serious problem. Site staff are spending more time managing paperwork than caring for patients or advancing the science behind the trial. This not only slows down study
Making Risk-Based Quality Management work in clinical trials
In the world of clinical trials, quality isn’t just about ticking regulatory boxes, it’s about protecting patients, ensuring data integrity, and running efficient studies. As trials become more complex, with multiple sites, endpoints, and technologies involved, Risk-Based Quality Management (RBQM) has become a key approach for sponsors and CROs looking to stay ahead. At the same time, modern tools like
The Role of CTMS in multi-site and international clinical trials
Running a clinical trial across several sites, or even across different countries, brings great potential, but also great complexity. With more moving parts, more regulations, and more people involved, keeping everything aligned becomes a daily challenge. That’s where a Clinical Trial Management System (CTMS) proves essential. At Xolomon, we work with sponsors and CROs who manage multi-site and international studies.
How to prepare your team to work with an eCRD system
As clinical trials become more digital, the adoption of electronic Clinical Research Document (eCRD) systems has become essential for sponsors, CROs, and research sites looking to improve data quality, streamline processes, and ensure compliance. But technology alone is not enough. To truly benefit from an eCRD platform like Xolomon, you need to make sure your research team is fully prepared
