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 and unexpected reactions with precision is critical.
Pharmacovigilance teams rely on consistent, complete, and timely data to detect safety signals. But too often, safety reporting is siloed from core trial operations, slowing down responses and increasing risk.
That’s where Xolomon can make a difference.
One platform, real-time safety visibility
At Xolomon, we believe that pharmacovigilance works best when it’s not an isolated function, but part of your digital clinical ecosystem. Our eCRD and CTMS tools allow investigators to record adverse events directly within the trial workflow, triggering alerts and ensuring full traceability across the system.
This means safety events are logged the moment they happen, no double entry, no delayed communication, no data slipping through the cracks.
Designed for compliance and audit readiness
From Good Clinical Practice (GCP) to ICH E2A and beyond, regulatory standards demand tight documentation of safety data. With Xolomon, all events are time-stamped, version-controlled, and auditable, so whether you’re preparing for an inspection or analysing cumulative safety profiles, your data is inspection-ready 24/7.
Our systems also support role-based access and event review workflows, ensuring that sponsors, CROs, and safety teams can collaborate transparently and securely.
Integrated safety, lower risk
By integrating safety reporting into your core clinical trial systems, you gain more than just convenience. You improve signal detection. You reduce human error. You cut the time from event to action, and that can make all the difference in protecting patients and complying with evolving regulatory demands.
In complex trials, it’s not enough to react. You need proactive systems that capture, route, and track safety data in real time.
Xolomon: making research accessible
Whether you’re launching a new molecule or monitoring post-marketing outcomes, pharmacovigilance depends on reliable systems. Xolomon offers the tools to ensure that every adverse event is seen, every response is documented, and every audit trail is intact.
Because safety isn’t optional and visibility is everything. Ready to strengthen your pharmacovigilance workflow?
