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.
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 and safety signals.
Our modular, end-to-end approach to drug safety reporting means we can improve every element of this process:
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. It 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.
Literature Review Services
Our literature monitoring team helps our customers with critical, time-consuming and resource-intensive tasks within the drug safety monitoring workflow.
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.
A TRUSTED PARTNER
We offer more than software and medical literature. We can partner with you to help with any element of drug safety monitoring, from constructing search strategies to outsourcing the entire literature review process.
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.
Biomedical Research Databases Available Through Dialog:
The Derwent Drug File selectively covers the worldwide pharmaceutical literature. Papers chosen may cover the chemistry, analysis, pharmaceutics, pharmacology, metabolism, biochemistry,...
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™ covers the fields of complementary or alternative medicine and allied health. Information is geared toward medical professionals, health practitioners and...
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...
MEDLINE is the U.S. National Library of Medicine (NLM) premier bibliographic database. It contains references to journal articles in life sciences with a concentration on biomedicine and health....
Get In Touch
We can help with all elements of medical literature monitoring, 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.