On-demand Webinar Recording: Improving Safety Reporting Speed and Accuracy with Automation and Embedded Intelligence

Access our on-demand webinar now

Hear from our expert speakers as we explore real-world case studies of how companies are utilizing intelligent process automation and embedded regulatory intelligence to improve the speed, accuracy and consistency of safety reporting.

You can register online and access the 30-minute webinar recording here.

Discover how organizations are harnessing our 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.

Speakers

Karin van Dort

Associate Director, Product Manager, Pharmacovigilance - PharmaLex

Karin van Dort is one of the industry’s most experienced pharmacovigilance and regulatory compliance experts. As Product Manager for psiXchange, her responsibilities span customer implementations, regulatory intelligence, and driving the roadmap. Earlier, Karin held senior safety submission and compliance roles at Grünenthal Group, and key clinical research roles at Pfizer, Parke-Davis and Pharmachemie.

Tim Billington

Director, Digital Solutions - PharmaLex

Tim Billington is a seasoned executive leader within the pharmaceutical industry. With extensive project management and implementation lead expertise, Tim brings over 20 years’ top-level experience and a strong track record working in software and services. He works closely with the Digital Innovation team to ensure that client and prospect feedback is part of our software evolution.