On-demand Webinar Recording

Improving Safety Reporting Speed and Accuracy with Automation and Embedded Intelligence

 

For busy safety and clinical teams struggling with complex safety reporting requirements and limited resources, innovative technologies have been shown to dramatically increase the speed and accuracy of safety reporting processes and compliance – while reducing cost and effort.

On-Demand 30 min Your Desk!

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Karin van Dort

Product Manager psiXchange & psiQ, Cencora PharmaLex

Tim Billington

Head of Business Development, Cencora PharmaLex

Join us to explore real-world case studies of companies utilizing intelligent process automation and embedded, regularly updated safety reporting regulatory intelligence of psiXchange software to:

  • Draw on embedded, up-to-date clinical trial safety reporting requirements with a comprehensive PV regulatory intelligence to improve the speed, accuracy, and consistency of safety reporting
  • Automate the end-to-end distribution, tracking, and acknowledgement receipt process for business-critical clinical trial safety documents to Sites, Ethics Committees, Competent Authorities, Notified Bodies, and Institutional Review Boards in more than 55 countries – reducing time, effort, and cost
  • Obtain an overview and detailed reporting of all relevant safety information per study and site in real time from a central “source of truth,” increasing safety oversight and regulatory compliance
  • Improve regulatory compliance and site responsiveness rates to as much as 90% (and higher for some customers), while saving up to 80% on operational costs involved in safety reporting

The result? Companies are automatically distributing the right safety document to the right recipients in the right format at the right time – freeing busy safety and clinical teams to focus on other critical tasks.

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