Pharmacovigilance (PV) Literature Monitoring with Intelligent Automation
A modular, end-to-end approach to literature surveillance for pharmacovigilance
Pharmacovigilance (PV) Literature Monitoring with Dialog Solutions
A modular, end-to-end approach to literature surveillance for pharmacovigilance
Streamlined approach
Our pharmacovigilance (PV) literature monitoring solution gives any organization tasked with drug safety reporting a streamlined, efficient and compliant approach to the entire literature triage process.
Comprehensive scientific and medical literature
Pharmaceutical companies of all sizes, contract research organisations, medical device manufacturers, biotech and biopharma firms use our solution to identify and review articles for Individual Case Safety Reporting, Aggregate Reporting (including PBRER, PSUR and DSUR) and Safety Signals detection.
Modular, end-to-end approach
Our modular, end-to-end solution for literature monitoring for drug safety means we can improve every element of the process.
Features and benefits
Comprehensive literature coverage
Dialog provides access to over 140 content databases, including MEDLINE, Embase and Biosis. We also standardize all our medical literature database content to provide a consistent search experience, eliminating the need for complex post processing.
Intelligent automation
The DialogML relevancy ranking engine is part of the Dialog system and uses Artificial Intelligence to apply a patient safety relevancy ranking to each reference in your Dialog search alerts results. DialogML ranking and highlighting of the key safety concepts help reviewers in Drug Safety Triager identify the most relevant articles first and reduces the review time per reference.
Improved efficiency
Drug Safety Triager delivers measurable efficiency and cost savings, while increasing productivity and compliance. The automated workflow ensures all articles are methodically ingested, processed and outputted for drug safety issues.
Advanced alert management
The search and alerts manager built into our pharmacovigilance monitoring solution makes it easier to manage and schedule multiple drug safety searches.
Precision search
Through our search platform Dialog, we offer precision search in our medical literature databases. Search results are output into a native XML format so they can be integrated seamlessly into drug safety reporting ecosystems.
Validated solution
Our Drug Safety Triager system is fully validated and compliant with the reporting requirements of global safety regulatory agencies such as the FDA, EMA and PMDA.
Our solutions
Dialog®
The Dialog platform delivers a consistent search experience across multiple databases, ensuring all relevant drug safety results are identified. With precision search, deduplication and quality XML output, Dialog is the industry standard for searching medical literature.
Dialog® Alerts Manager
The Dialog Alerts Manager simplifies the process of automating and managing multiple drug safety searches in Dialog. It also provides a range of features to meet the expectations of regulators and inspectors, such as an audit trail of search strategy setup and changes and alert delivery history.
Dialog®ML
DialogML is part of Dialog and uses artificial intelligence to make the literature review process quicker, more efficient and more thorough. DialogML enhances Dialog alerts by identifying references in scientific literature that meet the criteria for ICSR, Aggregate Reports or Safety Signals and applying a patient safety relevancy ranking to each reference and specific drug safety tags.
Drug Safety Triager™
Literature articles retrieved by the Dialog Alerts Manager are integrated directly into Drug Safety Triager. The system streamlines the literature monitoring workflow by eliminating duplicated content, reducing the volume of literature to be reviewed and automatically outputting literature references relevant to patient safety issues.
Drug Safety Triager and AI
Drug Safety Triager adds artificial intelligence assistance to the literature review process and increases the efficiency of review without introducing additional risk by prioritizing the review of the most relevant references first. It also gathers evidence for continuous algorithm improvement, paving the way for future phases of automated submission of the most relevant articles and elimination of the most irrelevant articles.
Literature Screening Services™
Our literature monitoring team helps our customers with critical, time-consuming and resource-intensive tasks within the drug safety monitoring workflow.
Get in touch
See how we can help your business.