Qscan® uses innovative algorithms and sophisticated analysis tools allowing you to generate safety signals from
adverse event data earlier and faster than ever before.
Targeted for both pharmaceutical and biotechnology firms required to monitor
the safety aspects of their drugs, Qscan offers a suite of products to effectively address these needs.
- Qscan®-ERM - THE System for Enterprise Risk Management A dedicated and complete system of three integrated components:
- A workflow module particular to drug safety
- A data browser for internal and external databases
- A world-class set of research tools.
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- Qscan®-FDA gives you access to the more than three million adverse event cases reported to the FDA (AERS), and made available through the
Freedom of Information Act. Using proprietary mapping tools and techniques, DrugLogic presents the data in a more usable way, and provides
sophisticated tools to interpret the findings.
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- Qscan®-VAERS gives you access to more than 300,000 vaccine adverse event cases reported to the Center for Disease Control.
- Qscan®-World is similar to Qscan FDA, but offers access to the CIOMS data provided by the Uppsala Monitoring Centre of the World
Health Organization (WHO), representing 67 countries.
DrugLogic® Services include reports, consulting, training, independent evaluations for pharmaceutical and insurance companies, CROs, medical schools and government agencies.
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