Increase Compliance PV

Achieve 100% compliance with drug safety reporting timelines while reducing localization costs by 30%

Join us in Milan 28-29 November for the European Pharmacovigilance Congress

To set up a meeting to discuss how we can support your multilingual safety requirements, please get in touch with one of our PV experts!

With TransPerfect Life Sciences, streamline the collection, processing, tracking, and reporting of cases as part of the pharmacovigilance process to increase quality and reduce spend.

TransPerfect’s Pharmacovigilance Practice Group can help you navigate increasingly complex regulatory environments to implement a more efficient process for multilingual safety reporting, including:

  • Global Call Center Support: Multilingual healthcare professionals for case intake and processing
  • Trial Interactive: 21 CFR Part 11 compliant solution developed for PV and safety management
  • GlobalLink Technology: 100% confidential and configurable solution to route safety content via appropriate translation workflows
  • AI for Translation: Safety-specific AI engines and human post-editors to reduce translation timelines by half
  • Redaction Services: AI technology and professional redaction specialists to reduce time to redact by over 50%
  • Media Monitoring for Safety: Technology to monitor digital media outlets in any language and provide meaningful reporting

Leveraging AI and Technology Now for Multilingual Safety Management

TransPerfect Life Sciences Blog


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