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With the increase in complexity of medical device manufacturing, data transparency and the case for quality initiatives become increasingly difficult to streamline and scale across the enterprise. This presentation will address quality best practices to maximize automated data science workflows to reduce root-cause analysis investigation cycle time, reduce reject rates, and increase process improvement to reduce complaints and adverse events.

In this webinar, we will cover:

  • Key challenges in the medical device industry
  • Overcoming quality barriers with an end-to-end informatics solution
  • Strategies to scale and optimize automated data science workflows
  • Implementing real-time assessment of quality to reduce reject rates
  • Decreasing root-cause investigation cycle time
  • And more...

Presented by:


  
  
  Kate Lusczakoski, PhD
  Director, BIOVIA Value Engineering
  Fellow, BIOVIA Science Council
  Dassault Systèmes BIOVIA




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Register for:

Scalable Quality Data Best Practices in Medical Device Manufacturing

Thursday, June 22, 8:00 AM - 9:00 AM Pacific Time

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