Adverse Event Reporting for Pharma & Biotech

Drug Safety Adverse Event Reporting

Sparta's adverse event reporting tracks reported events and manages the processing of cases from initial triage to reporting and case closure. Drug safety users can accurately and efficiently record events and products (suspect, company, prior, and concomitant), code terms against industry standard thesauri -- conduct seriousness, causality, and listedness/expectedness assessments -- and determine reportability of adverse events to appropriate health authorities.

For safety cases that are reportable, it supports a multitude of standard drug safety reports for paper and electronic reporting to meet expedited and periodic reporting requirements. 

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