Sponsored by:

Complimentary Webinar Recording
| Recorded on June 6, 2023 |

Mastering EU MDR:
Essential Strategies for Effective Risk and Document Management

REGISTER NOW!

Risk & Document management is an essential part of the MDR process.
Join this webinar to understand the risk management process, key requirements of MDR and best practices for compliance.

WHAT YOU'LL LEARN:

  • How to adopt a risk based approach (Risk analysis)
  • How correct documentation can save time to market (New/Existing Products)
  • How Our Client (Early adopters) were able to save 6 months by leveraging the right tools
  • Key learnings from experts so you can ensure your product gets to market faster

WHO SHOULD ATTEND:

  • SxMD, SaMD, SiMD
  • Medtech companies within 25-500 employees
  • RA/QA
  • Software Engineers, C Suite, Medtech, Regulatory Specialists

SPEAKERS

Ann Vanrukelsven

Ann Vanrunkelsven
RA/QA Manager
Matrix Requirements

Ann Vankrunkelsven is a driven and dynamic RA/QA professional who thrives on new challenges and making a positive impact in the world. With a PhD in Bio-engineering, she has always been fascinated by the intersections of science, innovation, and business. After years of honing her skills in Regulatory Affairs and Quality Assurance, Ann has become a true master, often lecturing at Ecole Polytechnique de Louvain. Currently RA/QA Manager at Matrix Requirements, Ann is a trailblazer who never settles for the status quo. She is passionate about helping customers & businesses succeed with Regulatory Affairs and Quality Assurance & firmly believes that improvement of the quality system and implementation of regulations need to stay practical to be successful.

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