Complaint and Adverse Event Handling Software
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InfoMed 9i is a start-to-finish tool for handling complaints and reporting adverse events.
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Uses built-in decision trees to guide you through event reportability.
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Includes full eMDR module for AS2 electronic submission to the FDA.
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Includes powerful smart tools like user configurable workflow rules and eNotifications for efficient and effective management of complaints and adverse event reporting activities.
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Is web-based and can be conveniently accessed globally, including from mobile devices.
