The question many Market Authorisation Holders (MAH) are asking themselves at the moment is how they can use artificial intelligence in pharmacovigilance literature review. The reason? Many MAHs...
Seeing double: eliminating duplicate references in drug safety literature screening
Drug safety literature screening for patient safety issues is not easy an easy process. As we saw in our post on keeping literature monitoring searches up to date, it can be hugely time-consuming...
Staying alert: how to easily update search alerts for drug safety literature monitoring
If it isn’t documented, it doesn’t exist. As far as regulators are concerned, this is true for any of the drug safety literature monitoring search alerts that a marketing authorisation holder (MAH)...
Introducing the next-generation of pharmacovigilance literature monitoring: Drug Safety Triager
As you might already know, Drug Safety Triager is our pharmacovigilance literature screening solution, designed to help pharmaceutical companies meet their regulatory requirements. It is already...
AI for Pharmacovigilance Literature Monitoring: Introducing DialogML
We’ve spoken before about using automation and artificial intelligence (AI) for pharmacovigilance literature monitoring. We’ve also discussed the benefits automation adds to our end-to-end medical...
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...
[VIDEO] How to deploy resources effectively in pharmacovigilance literature monitoring
When it comes to identifying patient safety issues relating to drugs, scientific and medical literature is a crucial resource. Get pharmacovigilance literature monitoring wrong, and you could draw...
How our end-to-end pharmacovigilance literature monitoring works [VIDEO]
At Dialog Solutions, we work with some of the world’s biggest pharmaceutical companies to deliver modular, end-to-end medical literature monitoring for pharmacovigilance. What’s more, we’re the only...
Why Quality Management and Validation Matter for Medical Literature Monitoring
“It is not enough to do your best; you must know what to do, and then do your best”. So said W. Edwards Deming, quality guru and founder of the concept of continuous improvement that transformed...