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International Clinical Trials

Accelerating Processes and Enhancing Compliance with Pharmacovigilance Automation

Adverse event (AE) information comes from healthcare professionals, manufacturers, and patients themselves, producing a huge volume of data to analyse. Life science organisations face a daily challenge capturing this information, assessing its significance, and reporting it to the authorities in a timely manner, so that safety information can be updated and, if appropriate, additional action can be taken.

It is clear that pharmaceutical companies should be harnessing the latest technology to capture and process the workloads. The range of technology options are considerable, and the technology is proven, reliable, and highly cost-efficient. However, it does appear that companies could be doing so much more with technology.

Many pharma companies believe they are making good use of technology for AE data capture and reporting, according to a recent survey. The research examines life science companies’ attitudes towards, and plans for, pharmacovigilance (PV) automation, particularly

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Dr John Price, owner and Managing Director of John Price PharmaSolutions LLC, is a life science regulatory and safety veteran and consultant, and an advisor to PV managed service provider Arriello.
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