How Leaders Are Preparing For EU MDR

On-Demand Webcast

What is the role of digitalization for medical device manufacturers? How are life sciences innovators preparing for new regulatory mandates, including the European Union Medical Device Regulation? And which key characteristics that distinguish life sciences leaders from laggards? Join Aberdeen analyst Greg Cline and PTC Senior Product Manager Mike Prudhomme as we review insights drawn from the 2018 PLM Digitalization Survey for Life Sciences. You’ll also learn how PTC is helping life sciences leaders adopt a sustainable product development approach that simplifies EU-MDR submissions.

In this webinar you’ll learn:

  • The fundamental role of digitalization in supporting medical device manufacturing
  • How life sciences leaders are preparing for EU-MDR (European Union Medical Device Regulation)
  • The PTC approach to creating a sustainable model for product development and regulatory submissions
  • IoT use cases specific to medical devices
  • How well your peers are meeting their quality, revenue and launch date targets
  • The persistent gap between compliance and quality -- what the data shows

Knowledge is power. In this webinar you’ll gain insights into the practices of life sciences leaders that can help you take practical steps to improve core life sciences product development processes – tackle the seismic shifts underway with EU MDR, and avoid common digitalization pitfalls.