QUOSA - Pharmacovigilance and drug safety

Pharmacovigilance and drug safety professionals

You need to screen scientific literature and triage for adverse events related to your products so that they can be promptly reported for regulatory compliance.

QUOSA provides the tools necessary to establish a product literature database for organizing and storing relevant articles for PSURs, ICSRs and other compliance reports.

Key benefits


Rapid identification of adverse events
Use alerts to monitor AEs reported in literature.


Monitor a broad spectrum of literature sources
QUOSA supports many third-party literature databases, including Elsevier and non-Elsevier content.


Automate the literature review and triage process
QUOSA allows article tagging and storage in a central library to facilitate a speedy and efficient process to triage articles and determine relevance for reports.


Implement sophisticated search strategies
Our experienced professional services team will work with you to make sure your searches capture appropriate literature for regulatory compliance.


Reduce development and administrative costs with a scalable central library
Store and organize literature in a scalable and secure "cloud-based" environment.


Manage high volumes of content
QUOSA automates the process of de-duplicating and organizing full-text literature.



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