Ensuring Efficiency and Compliance | Industry Spotlight Series – Medical Devices

How one medical device company eliminated manual work & improved training compliance

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Stop chasing training sign-offs and retyping complaint details. In this customer-led webinar, hear from Diane Shay, VP of Operations at a medical device company, as she shares exactly how they implemented Propel to modernize quality operations.

KEY TAKEAWAYS

Learn how Diane and her team:

  • Automated training compliance, eliminating manual sign-off tracking
  • Saved ~1 hour per complaint through streamlined intake and reduced data re-entry
  • Reduced reporting determination time from days to immediate access
  • Sustained audit-readiness and support for FDA eMDR timelines