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Complimentary Webinar

March 4, 2024 | 11:00 am ET (US) | 16:00 UTC

Launch Medical Devices to Market in the EU vs the US

REGISTER NOW!

Join us for a discussion on Essential Strategies to navigate the regulatory landscape and ensure you get your device to market on time and with the right tools.

WHO SHOULD ATTEND:

  • Quality, Regulatory, Engineering, Software and R&D staff who are involved in the preparation and entry into the European and American Markets

WHAT YOU WILL LEARN:

  • Common pathways to market in the EU & US
  • Regulatory strategies you need to consider
  • Key tools to help you avoid double work when creating documentation to different markets

SPEAKER

Vankrunkelsven_Ann

Ann Vankrunkelsven
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. An entrepreneur at heart, Ann built her own business, VR Projects which aims to help global businesses understand Regulatory and Quality Affairs.

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