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:
Shorten drug alert set up time by 80%
Decrease the time spent monitoring literature for aggregate reports and safety signals by 80%
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:
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.
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.
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.
Streamline Your Medical Literature Monitoring: Free Resources
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 watch the recording of 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:
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.
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.
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:
Morressier provides unique coverage of posters and abstracts from medical, engineering and life science conferences held around the world since 2015. Morressier aims to help scientists accelerate...
Derwent Drug File selectively covers the worldwide pharmaceutical literature. Papers chosen may cover the chemistry, analysis, pharmaceutics, pharmacology, metabolism, biochemistry, interactions,...
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...
Allied & Complementary Medicine™ Database covers the fields of complementary or alternative medicine and allied health. Information is geared toward medical professionals, health practitioners...
International Pharmaceutical Abstracts (IPA) provides comprehensive coverage of worldwide pharmacy literature. Such literature refers to articles on drugs and their properties, pharmacokinetics,...
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...
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.