About this webinar:

In this 30-minute pre-recorded webinar, Head of UL Global Medical Device Services, Sue Spencer shares her expertise in what to expect from a business standpoint for the new EU IVD Regulations.

The European Union IVD “revolution” has been in motion since 2012. Many of the larger companies are already putting the systems and requirements in place to prevent any interruption of business as we are now in final stages of finalizing through the EU Legislative process and expect the transition phase to begin as early as late 2016.

This Executive Brief addresses the key items your leadership team needs to know to understand the business impact the new regulations will have on the ability to sustain IVD sales in the EU.

Learn more about UL’s Notified Body services.

Contact UL: Medical.Inquiry@ul.com

Please Note: This webinar was recorded Tuesday June 28th, 2016.


Register to view the recording: