Preparing for EU MDR Product Submissions: A Sustainable Approach

For many medical device companies, complying with the new EU MDR regulation will require copious effort due to product data requirements being far more stringent than in the past. The time is now for companies to invest the time and resources to restructure processes and implement technology to streamline product related workflows.

This eBook from Tech-Clarity provides insights to companies preparing product data for regulatory submissions through a programmatic and extensible approach. In this view, EU MDR compliance serves as a catalyst for implementing sound product design, change, and configuration control best practices across your product development lifecycle.

Learn from others navigating these challenges:

  • Michelle Boucher | Vice President & author of eBook, Tech-Clarity
  • Caroline Byrd | Director of Regulatory Affairs, Abbott
  • Jay Crowley | VP & UDI Practice Lead, USDM Life Sciences
  • Dave Hadfield | Partner, Kalypso
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