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Overview What You Will Learn Webinar Speakers Who Should Watch?

Watch Now: Beyond the Spreadsheet: The Silent Cost of Data Chaos in Regulatory Affairs

Regulatory teams in the pharmaceutical industry face mounting pressure to manage increasingly complex datasets while staying compliant with evolving global requirements. Yet many organizations still rely on outdated tools like spreadsheets and siloed systems – creating inefficiencies, compliance risks, and escalating costs.

In this on-demand webinar, our expert examines the hidden costs of regulatory data chaos and outlines practical solutions to modernize processes. Learn how technology-enabled approaches can transform data management, reduce compliance costs, and enable regulatory affairs teams to focus on strategy rather than firefighting.

 

Why Watch

If your team is still struggling with fragmented data, manual tracking, and rising compliance costs, this session will help you identify opportunities for efficiency and long-term cost reduction. Move beyond the spreadsheet and take the first step toward scalable, future-ready regulatory operations.

Watch the webinar recording now and learn how to reduce compliance costs while regaining control of your regulatory data.

Where

Online Webinar

When

March 12, 2025 | 10:00 AM ET

What You Will Learn

Key Discussion Points

  • The true costs of manual spreadsheets in regulatory operations
  • Common compliance pitfalls caused by data fragmentation
  • How regulatory data chaos increases submission timelines and resource strain
  • Technology-driven solutions that streamline data management and improve traceability
  • Real-world examples of how pharma companies are reducing compliance costs year over year

Webinar Speakers

Manager, Regulatory Data Management

John Popp

John Popp brings deep expertise in xEVMPD, IDMP, RIMS, and global Regulatory Affairs. He has helped numerous pharmaceutical companies transform their regulatory operations—implementing the right systems, extracting and cleansing data, streamlining documentation processes, and enabling high-impact digital change. His insights are grounded in real-world implementation experience and a practical approach to regulatory innovation.

This session is designed for professionals in:

  • Regulatory Affairs & Operations
  • CMC & Technical Writing Teams
  • Quality & Compliance Functions
  • Data and Regulatory Systems Management