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Medicinal product safety teams are under enormous pressure to control ever-increasing caseloads, new sources of signal detection data, and changing regulations—all with flat budgets and resources. What if you could alleviate this pressure on multivigilance activities, while improving efficiency and strengthening compliance?
Collaborate with industry peers to advance safety.
Reduce processing time by 50% while improving accuracy and compliance through AI-powered digital case intake.Explore Safety Case Intake
Relieve the pressure of growing caseloads while maintaining compliance with global regulations and standards by automating safety case management.Explore Argus—Safety Case Management
Automate safety-signal detection with proven algorithms developed by world-class statisticians and data scientists.Explore Empirica—Safety Signal Management
“When you have Argus, you know you can handle everything from small Phase I to large Phase III and IV trials.”
Vice President, Services, Crown CRO
Medical device safety reporting requirements vary by region—make sure you are up to date on the regulations and are prepared to comply.Read the complete post
In an effort to bolster pharmacovigilance programs, pharma companies have succeeded in gathering massive amounts of data—so much so that they have found themselves struggling under the weight of it, particularly around adverse event reports. Is AI the solution?
Discuss best practices in pharmacovigilance, hear about harmonized approaches to meeting new regulatory requirements, and stay current with the Oracle safety product strategy and roadmap.
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Contact us about clinical research and pharmacovigilance.