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