ARISg™

Global Adverse Event Reporting System

The market leading software for Pharmacovigilance and Safety*, ARISg is the most advanced software solution for global safety surveillance available today. Supporting the collection of adverse events from all sources including spontaneous and clinical safety reports, ARISg enables full compliance with the international regulatory adverse drug event & reaction reporting requirements for expedited and periodic aggregate reporting.

Adverse Drug Event & Reaction Reporting Software

ARISg offers complete support for the global collection, coding, assessment and reporting of adverse event data. The data entry is logically organized based on the activity of the user while the optional workflow module routes cases automatically, based on the company's case handling procedures.

The distribution server determines case reportability based on business rules defined by the administrator, automating the distribution of expedited reports such as the CIOMS, MedWatch and E2B.

*ARISg is the most widely deployed safety system with more than 120 installations throughout North America, Europe and Japan including more than 20 of the top 50 pharma and biotech organizations. The system is used to submit more individual safety reports to the authorities than any other safety system and is currently being deployed at 2 major Regulatory Agencies.