Pharmacovigilance (PV) Literature Review Software: Drug Safety Triager

Drug Safety Triager is our next-generation pharmacovigilance (PV) literature review software, created to help life sciences organisations meet their regulatory requirements. It streamlines literature screening workflows through automation, configurability and an intuitive user interface. Drug Safety Triager marks an evolution in drug safety literature monitoring, making the process more efficient, compliant and cost-effective.

Contact us today to see how Drug Safety Triager can become a central part of your pharmacovigilance literature monitoring workflow.

Drug Safety Triager is our GxP validated and audit-ready pharmacovigilance (PV) literature review software solution, created from the ground up to monitor literature for Individual Case Safety Reporting, Aggregate Reports and Signal detection. It makes the drug safety literature monitoring process more efficient, cost-effective and compliant. Our customers range from top 10 global pharmaceutical companies to small biotechs and Contract Research Organisations.

Using intelligent automation from our machine learning engine DELVE (part of the Dialog platform) and integration with upstream and downstream processes, Drug Safety Triager takes literature reviewing to a new level. It simplifies the process so that the review teams can focus on what matters most: patient safety.  

With Drug Safety Triager you can:

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Reduce your Aggregate Report and Safety Signal review workload by 70%

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Halve the volume of literature to be reviewed for ICSRs when using DELVE


5x


Identify reportable adverse events 5x faster with assistance from our machine learning engine DELVE

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Achieve complete compliance with literature monitoring and reporting regulations

Drug Safety Triager Benefits

Drug Safety Triager is an integral part of our end-to-end medical literature monitoring solution, working seamlessly with the Dialog®platform, Dialog ®Alerts Manager and our literature screening services. Find out more about our end-to-end approach to pharmacovigilance literature monitoring here. 

Drug Safety Triager Ad-Hoc Report Example

CONFIGURABLE AND EASY TO USE

  • Automatic import and work allocation means no reference is missed for review
  • A modern and intuitive user interface allows users to concentrate on article analysis and assessment.
  • Automatic audit-trail for each document
  • Full text, translation and author follow-up support with day 0 change upon upload
  • Workflows for global teams and global GVP regulations
  • Timeliness tracking and quality control
  • Compliant output: ICSR E2B R3 output to case processing, Aggregate Reports in Vancouver style and Safety Signals in line listing
  • Extensive ad-hoc reports for proactive operation monitoring, work status visibility and reporting, oversight, and reconciliation.

SUPPORTED BY ARTIFICIAL INTELLIGENCE

Dialog Solution’s artificial intelligence engine DELVESM is part of the Dialog platform. It uses Natural Language Processing to enhances Dialog alerts by automatically identifying references in scientific literature that meet the criteria for ICSR, Aggregate Reports or Safety Signals.

DELVE applies a patient safety relevancy ranking to each reference and adds drug safety tags. As a result, in the Drug Safety Triager the most relevant and time-sensitive references are presented at the front of the queue and have the drug safety relevant terms highlighted.

This allows review teams to better prioritise their workload, reduces the risk of late ICSR submissions and speeds up the review. With DELVE assistance, literature review teams can find ICSRs 5x faster and reduce the volume of literature to be reviewed for ICSRs by up to 50% without introducing additional risk.

LEARN MORE ABOUT DELVE HERE

Drug Safety Triager Reference List Multi-Select

INCREASED EFFICIENCY WITH ROBOTIC PROCESS AUTOMATION

Drug Safety Triager automatically imports references from Dialog and other literature providers. The system auto-deduplicates at import and consolidates references retrieved for multiple drugs. Additional manual deduplication allows users to further reduce articles that need to be reviewed.

An automated workflow ensures references can be reviewed step-by step by multiple users for multiple purposes in an organised and transparent way. Automated work allocation and advancement of articles with step validation checks along the process enable all users to work independently and with full accountability.

FULL OVERSIGHT AND ADMINISTRATIVE CONTROL

Drug Safety Triager features a range of configurable dashboards that help increase oversight of even the largest drug safety monitoring workflows. The dashboard cards provide quick access to targeted statistics for an immediate view of work status, including potential risks, priorities and longer-term trends in the review workflow. Easy to use, configurable features allow the administrator role to be performed by either a business or an IT professional.

Administrator self-serve features, including:

  • Self-setup and configuration by the administrator
  • Full control over account creation and user access
  • Admin changes audit trail
  • Ad-hoc importing of additional literature outside of scheduled alerts
Drug Safety Triager Reference List

EFFICIENCY AND COST-SAVINGS 

Drug Safety Triager is proven to deliver measurable efficiencies and cost savings through: 

  • Deduplication 
  • Multi-drug review  
  • Bulk review
  • Easily accessible SOP links and supporting documents
  • An intuitive and streamlined interface  

The best-practice workflow reduces irrelevant literature references to be reviewed for Aggregate Reporting and Signal detection by up to 70%. 

 

GxP COMPLIANT PHARMACOVIGILANCE (PV) LITERATURE REVIEW SOFTWARE

Dialog Solutions’ Quality Management System provides the framework to consistently deliver products and services that meet customer and regulatory requirements. We are ISO 9001:2015 certified within the scope of Medical Literature Monitoring Solutions.

Each implementation of Drug Safety Triager is delivered with a validation package. The validation process and associated documentation are in line with pharmaceutical industry and health authority regulations.

All literature references undergo a systematic review process which automatically captures all users’ actions and adds a permanent, non-editable audit trail to the record. This process ensures audit readiness for any organisation using Drug Safety Triager.

ISO 9001:2005 Logo
Example of Full Text Acquisition with Article Galaxy on Drug Safety Triager

INSTANT ACCESS TO FULL-TEXT ARTICLES

Through the integration between Drug Safety Triager and Article Galaxy from Reprints Desk, full text acquisition is completely seamless. Literature reviewers can instantly access the full-text article needed for review, quickly upload it to the reference and update the day 0 date, further increasing efficiency and reducing the chance of errors. 

How Drug Safety Triager Works

Pharmacovigilance literature monitoring workflow

Introduction to Drug Safety Triager

Take a look at this short video for an overview of our flagship pharmacovigilance literature review tool, Drug Safety Triager.

In the video you’ll get a better understanding of how Drug Safety Triager works and how it integrates with our search platform, Dialog. 

You’ll also learn how Dialog and Drug Safety Triager together provide a fully-validated and audit-ready solution for medical literature monitoring.

Just click the play button on the video to get started! 

 

What Our Customers Are Saying

TOP TEN PHARMACEUTICAL COMPANY

Read a case study from one of the world's biggest pharmaceutical companies, looking at how it used our pharmacovigilance literature review software - Drug Safety Triager - to streamline its global medical literature monitoring for drug safety. 

MANAGER DRUG SAFETY SYSTEMS, TOP 50 PHARMACEUTICAL COMPANY

“We never before had drug safety software that worked from the first day with no errors and delivered the promised results”

DIRECTOR OF GLOBAL INFORMATION SERVICES

“With Drug Safety Triager we just completed an EMA audit; we have zero findings from the literature review process”

DIRECTOR OF GLOBAL INFORMATION SERVICES

“We have never experienced a more competent, more flexible and more responsive vendor”

HEAD OF LITERATURE SCREENING, TOP 10 PHARMACEUTICAL COMPANY

“Compared to what we had before, Drug Safety Triager is like going from a horse-drawn carriage to a space rocket”

Add Drug Safety Triager to Your Pharmacovigilance (PV) Literature Monitoring Workflow

Drug Safety Triager can integrate seamlessly with existing drug safety workflows. Contact us below to discuss how we can help you transform your approach to medical literature monitoring.