• [Webinar]Meeting New EU Medical Device Regulation Requirements With the PTC & Assent Platforms

    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. Join Travis Miller, Assent’s General Counsel, and Marc Fowler, PTC’s PLM Life Science Sales Leader, as they discuss how the PTC and Assent platforms work cohesively to acquire accurate, quality data that stands up to external scrutiny from regulatory and notified bodies.

    Register for the Webinar Today!

Meeting New EU MDR Requirements With the PTC & Assent Platforms — Webinar

Join this webinar to learn from product compliance experts about how to comply with new requirements under Section 10.4 of the EU Medical Device Regulation.%0D%0Ahttps://www.assentcompliance.com/assentu/resources/webinar/meeting-new-eu-medical-device-regulation-requirements-with-the-ptc-and-assent-platforms-200722/?utm_source=webinar-forward&utm_medium=email-forward&utm_campaign=BAU%0D%0AThe webinar is on Wednesday, July 22 at 11 AM ET. If you can’t make it, you can still register to receive a copy of the slides and recording.

TIME

11AM ET | 8AM PT | 3PM GMT

DATE

Wednesday July 22, 2020

DURATION

Approximately 60 minutes

Webinar Summary

You’ll learn 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 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:

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