• eu medical device

Meeting New EU Medical Device Regulation Requirements With the PTC & Assent Platforms

Webinar Replay


To meet new requirements under the European Union (EU) Medical Device Regulation (MDR), companies are engaging their suppliers for up-to-date information and reevaluating product composition. Hear from Travis Miller, Assent’s General Counsel, and Tony Funderburk, PTC’s PLM Sales Leader, as they discussed how the PTC and Assent platforms work cohesively to acquire accurate, quality data that stands up to external scrutiny from regulatory and notified bodies.

Attendees learned more about:

  • How Assent and PTC integrate to manage accurate product data.
  • The scope of Section 10.4 of the EU MDR.
  • How to work together with PTC and Assent effectively.
  • The support Assent offers to facilitate the process.

Don’t miss this opportunity to learn from subject matter experts with decades of experience in the field of product compliance!

Learn more about the PTC/Assent Integration:

  • Managing Product Compliance with the PTC & Assent Platforms
  • Managing EU Waste Framework Requirements With the Assent & PTC Platforms