Drug Delivery Business

New MDCG guidance on timelines and legacy device in Eudamed

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By Ronald Boumans, Emergo Group

New guidance from European regulators addresses data entry timelines for the Eudamed medical device database, as well as how to develop and assign Unique Device Identification (UDI) data for “legacy devices.”

Get the full story here at the Emergo Group’s blog.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of DrugDeliveryBusiness.com or its employees.

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About Danielle Kirsh

Danielle Kirsh is an award-winning journalist and senior editor for Medical Design & Outsourcing, MassDevice, and Medical Tubing + Extrusion, and the founder of Women in Medtech and lead editor for Big 100. She received her bachelor's degree in broadcast journalism and mass communication from Norfolk State University and is pursuing her master's in global strategic communications at the University of Florida. You can connect with her on Twitter and LinkedIn, or email her at dkirsh@wtwhmedia.com.