Automating Literature
Surveillance for Adverse Events

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Phamacovigilance Vertical Triangle
Phamacovigilance Vertical Triangle

DistillerSR for Pharmacovigilance

for Pharmacovigilance

Three of the top five pharmaceutical companies trust DistillerSR to automate literature triage and report on pertinent references with adverse events in an audit-ready, compliant, and real-time manner.

Why Companies Choose DistillerSR for Pharmacovigilance

Audit Ready Icon


Tracks 100% of your literature review. Integrated audit trail, version control, and data navigation mean your data is traceable.

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Smart & Fast

Identifies 95% of relevant records on average 60% sooner using AI reprioritization and predictive reporting.

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Always Up-To-Date Reviews

Automate adverse event tracking and monitoring from materials published daily to ensure patient safety and compliance.

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Works the way you do through 100% configurable workflows to support any protocol.

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Save Time

Reduces between 35%-50% of the time to complete your literature review by automating its every stage.


Exceeds expectations with a 92% CSAT rating and with 99% of customers renewing their subscription annually.

Learn More About DistillerSR

Learn More About DistillerSR

Featured Content

Pharmacovigilance Fact Sheet DistillerSR

Fact Sheet

Learn how PV specialists can use DistillerSR to automate literature surveillance and reporting that’s audit-ready and compliant.

Pharmacovigilance Product Video, DistillerSR


Watch how DistillerSR enables leading pharmaceutical companies to automate literature triage and reporting on adverse events.

AI Reprioritization Blog Post DistillerSR


Ian Stefanison, CTO for DistillerSR, answers questions on how AI reprioritization reduces screening times by as much as 80%, according to one study.

See DistillerSR in Action

See DistillerSR in Action