
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 paper, leading to time-consuming processes, storage challenges, and compliance risks. But things are changing. Today, more and more trial teams
Lo más leído

Why small sites need a CTMs too

Regulatory readiness: How to keep your trial systems inspection-ready 24/7

How to prepare your team to work with an eCRD system
No te pierdas lo último de Xolomon

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 paper, leading to time-consuming processes, storage challenges, and compliance risks. But things are changing. Today, more and more trial teams are turning to digital tools to streamline operations and cut

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 a powerful tool in clinical research, allowing patients to report on symptoms, quality of life, or treatment effects in real time. Yet for many teams just getting started, one question

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 benefit the most from a well-implemented CTMS. Whether you’re a single-site team, an academic hospital, or a small CRO managing a handful of studies, a CTMS can provide clarity, structure,

Managing budgets and invoicing in clinical trials: why you need a CTMS
Clinical trials are complex by nature, scientifically, operationally, and financially. While much attention is given to data collection and patient safety, one critical element often underestimated is the management of budgets and invoicing. In multi-site, multi-phase trials, the financial side can quickly become unmanageable without the right tools. From tracking site payments to reconciling sponsor invoices, small inefficiencies can snowball