✓ QPPVs ✓ LPPVs ✓ GSOs ✓ CMOs ✓ RegIntel Teams ✓ QA Teams ✓ Auditors
with iViReg 100+ countries
iViTracker helps you manage every assessment with full compliance and a complete Audit Trail — regardless of where your data originates:
It provides a centralized platform for tracking adverse events, ensuring compliance with global regulatory requirements, and facilitating timely reporting. By automating and simplifying these processes, iViTracker helps organizations maintain high standards of patient safety and regulatory adherence.
Yes, you can request a live demo of iViTracker to explore its features and capabilities. This demonstration allows you to see how the platform can be tailored to your organization’s needs. To schedule your free demo, click here.
PV regulatory intelligence ensures organizations involved in medicinal product development and safety remain informed about local ADR reporting requirements, including what must be reported, timelines, submission formats, and language specifications. This knowledge is essential for maintaining compliance with national and regional regulations.
No matter what task you put in iViTracker, you can submit Tasks/Subtasks, Track Deadlines...and it is all recorded in an Audit Trail
No commitment required - just a clear insight into how it can benefit your pharmacovigilance operations.