Pharmacovigilance (PV) Literature Monitoring
Our pharmacovigilance (PV) literature monitoring solution offers a modular, end-to-end approach to literature surveillance for pharmacovigilance. It gives any organisation tasked with drug safety reporting a streamlined, efficient and compliant approach to the entire literature triage process.
Get in touch with us today to discuss how we can improve your approach to pharmacovigilance literature surveillance or take a look at the resources below.
At every stage of the medical literature monitoring process, we help our customers save time and money. Using our pharmacovigilance literature monitoring solution, our customers are able to:
Shorten drug alert set up and management time by 80%
Reduce the Aggregate Report and Safety Signal review workload by 70%
Identify reportable adverse events 5x faster with assistance from our machine learning engine DELVE
Halve the volume of literature to be reviewed for ICSRs when using DELVE
Achieve complete compliance with literature monitoring and reporting regulations
Pharmacovigilance (PV) Literature Monitoring with Dialog Solutions
Pharmaceutical companies of all sizes, contract research organisations, medical device manufacturers, biotech and biopharma firms use our drug safety literature screening solution to identify and review articles for Individual Case Safety Reporting, Aggregate Reporting (including PBRER, PSUR and DSUR) and Safety Signals detection.
Our modular, end-to-end approach to drug safety reporting means we can improve every element of this process:
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.
Our Literature Search Services team can also create custom, regulatory compliant drug safety search strategies for your medical literature monitoring workflow.
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 audit trail of search strategy set up and changes and alert delivery history.
DELVE is part of Dialog and uses artificial intelligence to make the literature review process quicker, more efficient and more thorough.
DELVE 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. This means the most relevant and important references are presented to reviewers at the front of the queue helping them better prioritise their workload, find relevant articles more quickly, and speed up analysis and review.
Literature articles retrieved by the Dialog Alerts Manager are integrated directly into Drug Safety Triager, our next-generation GxP validated and audit-ready pharmacovigilance literature monitoring solution. It makes the drug safety literature monitoring process more efficient, cost-effective and compliant. 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 for patient safety issues.
In addition, Drug Safety Triager adds artificial intelligence assistance to the literature review process without introducing additional risk. 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.
Dialog Solutions Pharmacovigilance (PV) Literature Monitoring Features and Benefits:
The Dialog DELVESM 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.
The relevancy ranking score, together with highlighting of key safety concepts, help make the literature monitoring process more efficient and reduces literature reviewers’ workloads without introducing additional risk.
Drug Safety Triager, our validated pharmacovigilance literature triage solution, 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 ALERTS management
The search and alerts manager built into our pharmacovigilance monitoring solution makes it easier to manage and schedule multiple drug safety searches.
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 and compliant
Our medical literature monitoring solution is fully validated and compliant with the reporting requirements of global safety bodies, including the FDA, EMA and PMDA.
Streamline Your Medical Literature Monitoring: Free Resources
Pharmacovigilance (PV) Literature Screening: Best Practice Checklist
Click the button below to download our exclusive, 18-step best practice guide for optimising your drug safety literature screening process.
On-Demand Webinar: Manage growing literature review workloads with pharmacovigilance automation and integration
Literature review teams in drug safety departments are overloaded with a rising tide of work and decreasing budgets. The number of adverse events being reported is growing year on year, along with the amount of literature that needs to be monitored. For drug safety teams, this pace isn’t sustainable; they either need to employ more reviewers or run the risk of valid ICSRs being missed by overworked teams.
In our on-demand webinar we take a closer look at these issues and what drug safety teams can do to address them. By watching our on-demand webinar you’ll learn more about:
- The unavoidable challenge pharmaceuticals face from a growing literature review workload
- Why this workload is unsustainable
- What pharmacovigilance automation can do to streamline the literature review workload without adding risk
- How integration with downstream systems can improve the whole pharmacovigilance workflow
- How drug safety departments can prepare for the future of literature monitoring for product safety
Enter your details to watch the webinar:
Video Series: End-to-end literature monitoring in pharmacovigilance with Dialog Solutions
Take a look at these three short videos to see exactly how our end-to-end solution for medical literature monitoring works in practice. Between the three videos, you’ll get a better understanding of:
- How to use the Dialog platform to search for adverse events
- How to create alerts on Dialog to find adverse events
- What Drug Safety Triager, our drug safety literature monitoring tool, can do for your drug safety monitoring workflow
Get In Touch
We can help with all elements of medical literature monitoring for pharmacovigilance, saving you time and money as well as improving regulatory compliance and reducing the risk of missing patient safety alerts. Contact us using the button below to see how we can support you.