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LiveWorx 2019

LS113P - Preparing for EU-MDR: Insights from Medical Device Leaders

Session Description

The medical device industry is facing a wave of regulatory challenges, including EUMDR, GDPR, and Single Audit Program (MDSAP). The EUMDR 2020 deadline for the first wave of devices is rapidly approaching, and companies are moving from planning to action. Learn how life sciences leaders are rising to the challenge in this panel discussion. Panelists will explore a range of approaches for tackling common compliance challenges and highlight similarities and differences across companies.


Session Presenter
Additional Information
Life Sciences
Compliance & Regulatory Oversight
Learn how life science leaders are adopting sustainable compliance strategies.
Understand the critical role of PLM in streamlining regulatory processes.
Learn how peers in other companies are tackling common challenges.
Panel Discussion
45 minutes
Session Schedule