NEW YORK, September 14, 2016 /PRNewswire/ --
A New Version of QUOSA' Will Empower Rapid, Efficient and Transparent Literature Review to Save Time and Improve Regulatory Compliance
Elsevier, a world-leading provider of scientific, technical and medical information products and services, today announced it has updated its pharmacovigilance (PV) portfolio with the launch of QUOSA PV. This new version of Elsevier's QUOSA literature management solution is specifically designed for the monitoring and review of scientific literature for adverse drug events.
QUOSA PV, developed by PV experts for PV experts, is a tool that organizes and automates the monitoring and triaging of articles, and other forms of literature, in a scalable environment. It will help PV groups address patient safety, ensure transparency, maintain compliance with regulatory guidelines and improve the efficiency of the literature screening workflow. QUOSA PV, which also supports the EMA's Medical Literature Monitoring (MLM) program, delivers a user-friendly, browser-based interface, empowering rapid, transparent literature surveillance and case triage. In addition, it is qualified to operate in a Good Practice (GxP) regulated environment.
Efficiency and compliance
In order to meet regulatory requirements for monitoring various sources of literature for adverse drug events, PV groups may depend on purchased or internally developed systems. However, these applications are typically neither scalable nor specifically designed for PV, lacking sufficient search, triage and alert functions. Legislation from 2012 means the number of literature articles that must be processed is continually rising, resulting in identification of more adverse events (AE) than historically has been the case. As a result, more resources are needed to ensure all AEs are captured and evaluated rapidly, increasing the need for more efficient and structured workflow management for an increasing number of articles and alerts. Further, some existing tools used for literature review and triage also struggle to meet the stringent compliance demands in place for reporting AEs, such as the need to track review histories and demonstrate transparency in case of audits.
Integrate EMA Medical Literature Monitoring (MLM) service results into the review process
The European Medical Agency's (EMA) MLM program - which came into effect in September 2015 - requires PV groups to review daily reports from the EMA. These reports can be uploaded and cross-checked in QUOSA PV, reducing the need to use multiple tools, saving time and ensuring accuracy.
"The continually growing volume of published literature places extra demands on PV systems and teams. PV groups, information managers and drug researchers are constantly challenged to ensure patients' safety and regulatory compliance with regard to literature monitoring," said Günther Kurapkat, Head of R&D Solutions for Pharma and Life Sciences, Elsevier R&D Solutions. "QUOSA PV overcomes this challenge and addresses the key issues that are important to our customers by delivering a centralized triage tool that lets users be more confident they are not missing critical safety information."
Quality by design
The QUOSA PV tool is qualified to operate in a GxP regulated environment; it also offers a searchable and exportable audit trail to help with inspection readiness. By automating the process of deduplicating and organizing literature, the screening process is more cost effective and efficient. In addition, by reducing the burden of time spent sifting through large amounts of content and instilling confidence that all relevant information is identified and analyzed, PV groups can focus on their primary role of ensuring patient safety.
Find out more about QUOSA PV.
About Elsevier
Elsevier is a world-leading provider of information solutions that enhance the performance of science, health, and technology professionals, empowering them to make better decisions, deliver better care, and sometimes make groundbreaking discoveries that advance the boundaries of knowledge and human progress. Elsevier provides web-based, digital solutions - among them ScienceDirect, Scopus, Elsevier Research Intelligenceand ClinicalKey - and publishes over 2,500 journals, including The Lancet and Cell, and more than 35,000 book titles, including a number of iconic reference works. Elsevier is part of RELX Group, a world-leading provider of information and analytics for professional and business customers across industries.www.elsevier.com
Media contact
Christopher Capot
Director, Corporate Relations, Elsevier
+1 917 704 5174
c.capot@elsevier.com
