EU MDR: Best Practices for UDI Data & Product Labeling, Upcoming Webinar Hosted by Xtalks

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In this free webinar, featured speakers from Reed Tech and PRISYM ID will discuss what device companies will need to do to be EU MDR compliant. The discussion will focus on device registration, UDI data management and product labeling.

Xtalks Life Science Webinars

According to a recent survey*, most manufacturers realize the significant effort to transition from the EU Medical Device Directives to the Medical Device Regulation (EU MDR) and are continuing their EU MDR preparation activities.

On Thursday, February 20, 2020 at 10am EST (3pm GMT/UK), join Gary Saner, Sr. Manager of Information Solutions Life Sciences, Reed Tech and Richard Castle, Global Account Manager Medical Device at PRISYM ID for an informative live session. In addition to discussing the procedure, other topics include EU MDR timing deadlines, best practices in creating and submitting product data and best practices in preparing and maintaining compliant labels not only for EU MDR, but for the upcoming regulations, too.

According to a recent survey*, most manufacturers realize the significant effort to transition from the EU Medical Device Directives to the Medical Device Regulation (EU MDR) and are continuing their EU MDR preparation activities.

They understand:

1. The EU MDR “process” is not delayed
2. EU MDR compliant products must meet new labeling requirements as of the Date of Application (DoA) and
3. EU MDR documentation and device registration previously expected to be reported to EUDAMED must still be reported per corresponding Directive provisions in the two-year delay period

Accordingly, best practices are being followed for creating structured device registration and Unique Device Identification (UDI) data and for implementing EU MDR compliant product labels in order to comply with the EU MDR DoA requirements.

*Survey information

For more information or to register for this event, visit EU MDR: Best Practices for UDI Data & Product Labeling.

Reed Tech offers UDI solutions for Global Health Authorities. Click here to learn more.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

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Candice Tang
Xtalks
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