Pharmacovigilance
Automating Literature
Surveillance for Adverse Events
DistillerSR for Pharmacovigilance
for Pharmacovigilance
Why Companies Choose DistillerSR for Pharmacovigilance
Audit-Ready
Tracks 100% of your literature review. Integrated audit trail, version control, and data navigation mean your data is traceable.
Smart & Fast
Identifies 95% of relevant records on average 60% sooner using AI reprioritization and predictive reporting.
Always Up-To-Date Reviews
Automate adverse event tracking and monitoring from materials published daily to ensure patient safety and compliance.
Configurable
Works the way you do through 100% configurable workflows to support any protocol.
Save Time
Reduces literature review times by 35%-50% by automating every stage of
the process and by reusing already collected data.
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Integrated
Maintain a single source of truth by synchronizing literature review data seamlessly with your reporting applications and safety databases.
Learn More About DistillerSR
Learn More About DistillerSR
Featured Content
Pharmacovigilance Fact Sheet
Learn how PV specialists can use DistillerSR to automate literature surveillance and reporting that’s audit-ready and compliant.
Blog
Q&A Blog Post: How Can Automation Support Literature Surveillance for Pharma and Biotechnology?
Blog
Ian Stefanison, CTO for DistillerSR, answers questions on how AI reprioritization reduces screening times by as much as 80%, according to one study.