How to Ensure Compliance With the New EU Medical Device Regulations: MDR & IVDR, New Webinar Hosted by Xtalks

Xtalks Life Science Webinars

The new European Medical Device Regulations (MDR) and the In Vitro Diagnostic Medical Device Regulations (IVDR) represent some of the most wide-ranging and disruptive changes to recently affect the world’s second-largest medical technology market.

Now, with just a two- to four-year transition period before full compliance is required in 2020 for MDR and 2022 for IVDR, device developers will need to implement changes to help new and existing products succeed. The scope and complexity of this legislation will require significant changes in areas such as product development, data reporting, quality assurance and manufacturing processes. While these dates may seem a long way off, manufacturers need to start planning immediately, as adjusting will take time and effort.

Join Karen Hill, BSc (Hons), Senior Manager of Regulatory Affairs at ICON plc, on Monday, Sept. 17, 2018, at 1 p.m. EDT to learn:

  • The key changes that are occurring under the new regulations
  • How to prioritize product portfolios
  • The importance of early planning in preparing clinical studies to certify new devices and to recertify existing ones
  • How early transition can give products an advantage in the market

To learn more about this complimentary event, visit: How to Ensure Compliance with the New EU Medical Device Regulations: MDR & IVDR.

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/.

Contact:

Nima Rajan
Tel: +1 (416) 977-6555 ext 352
Email: [email protected]

Source: Xtalks

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Tags: EU MDR, ICON, IVDR, Medical Device Clinical Trials, Medical Device Safety and Regulation, Xtalks


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Xtalks is a leading provider of educational webinars to the global life science, food and medical device community.