Audience

Professional teams interested in a tool to streamline literature review workflows and ensure compliance with global safety regulatory requirements

About Drug Safety Triager

Drug Safety Triager is Clarivate's next-generation pharmacovigilance software designed to assist life sciences organizations in meeting regulatory requirements. This GxP-validated, compliant, and audit-ready system manages and streamlines the literature review workflow, enabling pharmacovigilance experts to focus on patient safety by simplifying literature review processes. The platform is fully validated and compliant with the reporting requirements of global safety regulatory agencies such as the FDA and EMA. Each implementation of the Drug Safety Triager is delivered with a validation package. The validation process and associated documentation align with the pharmaceutical industry and health authority regulations. All literature references undergo a systematic review process that automatically captures all users’ actions and adds a permanent, non-editable audit trail to the record.

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Company Information

Clarivate
United Kingdom
clarivate.com/life-sciences-healthcare/research-development/pharmacovigilance-drug-safety/drug-safety-triager/

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Product Details

Platforms Supported
Cloud
Training
Documentation
Live Online
In Person
Support
Phone Support
Online

Drug Safety Triager Frequently Asked Questions

Q: What kinds of users and organization types does Drug Safety Triager work with?
Q: What languages does Drug Safety Triager support in their product?
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Drug Safety Triager Product Features