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Complimentary Webinar Recording
| Recorded on June 6, 2023 |

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


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.


  • 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


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


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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