Detect Safety Signals Faster with Automated Literature Monitoring

Streamline your local literature monitoring and case review process, and receive multilingual case processing support.

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Pharmacovigilance (PV) & Safety Automation

Automated Local Literature Monitoring

Pharmacovigilance and medical information teams face increasing pressure to detect safety signals, review literature efficiently, and ensure compliance. Shorten adverse event reporting timelines with tailored AI-powered solutions that meet your needs. Using natural language processing (NLP), it scans vast volumes of global and local publications, applies consistent screening criteria, and detects emerging safety signals with exceptional speed and accuracy. 

Automation can help your team:

  • Manage high volumes of global and local publications

  • Maintain regulatory compliance on a global scale

  • Avoid duplicate, incomplete, or inaccurate database entries

  • Reduce the resource strain of manual monitoring

  • Track social media signals for 360° patient safety surveillance

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testing & quality assurance in training

Local Literature Search Services

Need hands-on support? Access end-to-end language services for pharmacovigilance literature surveillance—customized to meet your specific requirements.

Support services include:

  • Consultation on local publication and keyword requirements
  • Search strategy creation and localization for optimal surveillance
  • Custom automations to reduce manual review time
  • Flexible review and signal detection setup and support
  • End-to-end process centralization and activity tracking
  • Expert support for audit and inspection readiness
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Ensure Compliance with Good Pharmacovigilance Practices (GVP Module VI)

Automate manual processes to detect safety signals faster and respond quickly to adverse events. Help your pharmacovigilance team meet global regulatory requirements with automated multilingual case processing that connects seamlessly to your existing systems.

Discover how to stay ahead of GVP compliance timelines, scale social media and literature monitoring across regions and languages, and reduce operational costs with expert support and AI.

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The ROI of TransPerfect Literature Monitoring Solutions

85 %

Increase in operational efficiency by automating search and screening tasks.

24/7

Global support for uninterrupted literature reporting and compliance coverage.

100 %

Quality-controlled case reporting with secure systems and validated processes.

Ready to Automate Your Literature Review?

Save time, reduce risk, and scale faster in pharmacovigilance literature monitoring.

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