Medical Literature Monitoring

Our medical literature monitoring solution offers a modular, end-to-end approach to literature monitoring for pharmacovigilance. It gives any organisation tasked with drug safety reporting a streamlined, efficient and compliant approach to the entire literature review process. 

Get in touch with us today to discuss how we can improve your approach to literature monitoring for drug safety, or take a look at the free resources below

At every stage of drug safety monitoring process, we help the world’s biggest pharmaceutical companies save time and money. Using our medical literature monitoring solution, our customers are able to: 

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Shorten drug alert set up time by 80%

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Decrease the time spent monitoring literature for aggregate reports and safety signals by 80%

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Cut in half the time it takes literature reviewers to monitor literature for ICSRs

Medical Literature Monitoring with Dialog Solutions

Pharmaceutical companies of all sizes, contract research organisations, medical device manufacturers, biotech and biopharma firms use our medical literature monitoring solution to identify and review articles for relevant ICSRs, aggregate reports (including PBRER, PSUR and DSUR) and safety signals.

Our modular, end-to-end approach to drug safety reporting means we can improve every element of this process:

Content

We provide access to all essential content databases for pharmacovigilance through the Dialog® platform.

Dialog®

The Dialog® platform delivers a consistent search experience across multiple databases, ensuring all relevant drug safety results are identified. Our Literature Search Services team can also create custom, regulatory compliant drug safety search strategies for your medical literature monitoring workflow. 

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.

Drug Safety Triager

Literature articles retrieved by the Dialog Alerts Manager are integrated directly into Drug Safety Triager, our fully-validated, flagship drug safety monitoring tool. The system streamlines the literature monitoring workflow by eliminating duplicated content, reducing the volume of literature to be reviewed and automatically outputs literature references relevant to patient safety issues.

Our machine learning model makes the literature analysis even more efficient by helping the reviewers prioritise their work and focus on the drug safety elements of analysed 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.

Streamline Your Medical Literature Monitoring: Free Resources

Free Course: Learn How To Supercharge Your Pharmacovigilance Literature Monitoring

In this free four part course, we’ll share with you advice and guidance for making your pharmacovigilance medical literature monitoring more efficient, cost-effective and compliant. 

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 Japanese industry after World War II. With this maxim, Deming captured the essence of Quality* management and validation in the medical literature monitoring (MLM) software that is used in...

How to Reduce Missed Drug Safety References with Precision Search

Can a single missed drug safety reference be a billion dollar problem? If it’s been missed in literature monitoring for pharmacovigilance, it can. A missed drug safety reference can have serious consequences, with PV professionals making the wrong conclusions and patients being harmed, prompting lawsuits, regulatory action and precipitous share price falls. But when marketing authorisation...

Doing It Right: The Rigorous Approach to Medical Literature Monitoring for Drug Safety

Correctly identifying adverse events from medical literature is one of the key tasks in pharmacovigilance (PV). It’s also one of the most complex. The sheer volume of information available is overwhelming: so much so that even in the most precisely constructed searches, only five percent of references retrieved will be relevant. Then there’s the issue of duplicate articles, which on average,...

You Need to Reduce Duplicate References in Your Medical Literature Monitoring: Here’s Why

Too much information. In our everyday lives it’s an irritation, at worst. But in medical literature monitoring, it’s a major issue. How do you cut through the noise to find the reference that really matters? In our paper Better Relevance, we discussed how precision search can cut down the volume of alerts relevant to adverse events by 30-50%. But this alone doesn’t solve the information overload...

Can AI and machine learning automate medical literature monitoring?

If you work in pharmacovigilance (PV), are the robots coming for your job? Medical literature monitoring is part of the PV process with significant scope for automation. On the face of it, this seems an obvious insight. Literature monitoring ticks all the boxes for needing to be automated. It can be repetitive, time-consuming work that ties up experts who could be spending more time on patient...

 

Webinar: Three Ways To Improve Your Approach to Medical Literature Monitoring

Our webinar looks at three key areas in medical literature monitoring – search, duplicate references and quality and validation – and provides advice and guidance on how you can optimise each of these elements in your medical literature monitoring process. 

By the end of the webinar you’ll have a better understanding of the impact search strategies, duplicate references and validated software has on the efficiency and effectiveness of your medical literature monitoring workflow. Click the link to register for the webinar. 

 

Checklist: Benchmark your Pharmacovigilance Literature Monitoring

We’ve created a best practice guide to help you benchmark your approach to medical literature monitoring. This 18 step checklist looks at search, duplicates and quality management, and provides guidance as to what best practice should look like for each of these areas.

Download the guide for a handy checklist that will help you identify the areas in your medical literature monitoring process that can be made more efficient, cost-effective and compliant.

Dialog Solutions Medical Literature Monitoring Features and Benefits:

Comprehensive literature coverage

We provide access to over 140 content databases, including Medline, Embase and Biosis. We also standardise all our medical literature database content to provide a consistent search experience, eliminating the need for complex post processing.

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.

Improved Efficiency

Drug Safety Triager, our validated literature monitoring 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 search management

The search and alerts manager built into our pharmacovigilance monitoring solution makes it easier to manage and schedule multiple drug safety searches.

Artificial Intelligence

Our medical literature monitoring solution uses machine learning to improve the quality, speed and efficiency of the literature review process by automatically identifying articles that qualify as ICSRs.

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. 

Dialog Biomedical Databases:

Derwent Drug File

Derwent Drug File selectively covers the worldwide pharmaceutical literature. Papers chosen may cover the chemistry, analysis, pharmaceutics, pharmacology, metabolism, biochemistry, interactions,...

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Pharmaprojects

Pharmaprojects is the complete drug intelligence service covering global drug research and development across all disease areas since 1980. It sets the standard for comprehensive intelligence about...

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Allied & Complementary Medicine

Allied & Complementary Medicine™ Database covers the fields of complementary or alternative medicine and allied health. Information is geared toward medical professionals, health practitioners...

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International Pharmaceutical Abstracts

International Pharmaceutical Abstracts (IPA) provides comprehensive coverage of worldwide pharmacy literature. Such literature refers to articles on drugs and their properties, pharmacokinetics,...

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SciSearch

SciSearch: A Cited Reference Science Database is not only a large, multi-disciplinary, international bibliographic database covering 150 disciplines in science, technology and biomedicine, but also...

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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. 

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