In clinical research, no two studies are exactly alike. Some run smoothly from start to finish. Others change course halfway, adapt their protocols, or need rapid amendments across multiple sites.
That’s where flexible eCRFs make all the difference.
More than custom fields: adaptability in real time
Most electronic case report forms (eCRFs) allow users to customise fields, validations, and visit structures. But when the complexity of a trial increases, for instance, in adaptive designs, multicentric studies or evolving protocols, not all systems offer the same level of flexibility.
Xolomon’s eCRF stands out by giving researchers the power to:
- Adapt forms mid-study, without compromising existing data
- Create dynamic workflows that respond to the trial’s progress
- Scale across centres or phases without reconfiguring the whole system
- Implement complex validation logic without external development
In other words: it’s not just that you can customise your eCRF, it’s how quickly, easily and safely you can do it.
Designed for change, built for clarity
In fast-paced research environments, delays in implementing protocol changes can mean data loss, compliance issues, or patient disengagement. That’s why Xolomon’s eCRF was designed for teams that need to stay agile:
- Changes are applied through an intuitive interface, no need to rely on long dev cycles
- Every update is fully traceable and compliant with regulatory requirements
- Sites and monitors can adapt instantly to new structures, validations or visit rules
With Xolomon, you’re never locked into a rigid structure, because clinical trials aren’t static either.
Why CROs and sponsors choose flexibility
Whether you’re managing a small investigator-led study or a large multinational trial, flexibility allows you to move faster, correct sooner, and gather higher quality data.
That’s why more and more CROs and sponsors trust Xolomon when customisation isn’t just a feature, it’s a necessity.
Ready to see how it works? Book a demo with Xolomon.
