Oracle Adverse Event Reporting System

Manage Adverse Events and Reduce Risk

Provides pharmaceutical companies with the power to store and monitor adverse events encountered in clinical trials so that safety concerns can be addressed before a drug reaches the market.

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  • Query all adverse event and complaint data from one simple interface
  • Utilize powerful case management features
  • Produce regulatory reports from standard templates
  • Use Submission Wizard to determine reporting requirements
  • Monitor safety issues over time using audit trail and tracking
  • Easy to use interface
  • Powerful functionality at the touch of a button
  • Clear visibility into data
  • Saves time
  • Simplifies safety monitoring and compliance
Video: Oracle Health Sciences Product Safety Suite (1:50)
More about Oracle Health Sciences

Oracle delivers key functionality built specifically for pharmaceutical, biotechnology, clinical, and medical device enterprises. With Oracle, you maximize your chances of discovering and bringing to market products that will generate profits quickly.

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