October 6th, 2016

PRE-RECORDED WEBINAR: 66/585/FDIS – IEC 61010-1 3rd Edition – Amendment 1

In this 30-minute pre-recorded webinar, UL Principal Engineer, Walter Hofmair shares his expertise live with an audience, on the major changes in the Final Draft of Amendment 1 to IEC 61010-1, 3rd edition. Mr. Hofmair actively participates in the Interenational Standards, IEC Technical Committees and Working Groups for “Safety of Measuring, Control and Lab Equipment.”… read more

August 26th, 2016

PRE-RECORDED WEBINAR: Broader Regulatory Oversight of In Vitro Diagnostic Devices: A Deep Dive into the changes to the EU IVD Regulations

The European Union has recently published the new IVD Regulations which are distinct and separate from the Medical Device Regulations. The revised IVD Regulations have been modified so extensively that it is estimated that whereas now 20% of IVD’s are under EU Regulatory control, when enacted, almost 80% of IVDs will be under regulatory control…. read more

August 25th, 2016

UL experts share safety lessons for injectable devices

A recent article by UL Human Factors Engineering experts, Michael Wiklund and Allison Strochlic, published online in MedTechIntelligence highlights key safety lessons learned regarding safe design of injectable devices. The authors go into detail on the following five areas: Lesson 1: Apply Human Factors Engineering Throughout Development Lesson 2: Avoid These Specific Use Errors Lesson 3:… read more

August 19th, 2016
PRE-RECORDED WEBINAR: Changing In Vitro Diagnostic Device Regulations: A Deep Dive into the New EU Requirements for Clinical Evidence
July 29th, 2016
UL Featured in Popular DC Podcast
July 19th, 2016
UL Article published on 3D Printed Devices
May 6th, 2016
UL continues to Lead in the Issuing of IECEE CB Certificates in MED and MEAS Categories
March 22nd, 2016
US FDA Medical & Combination Product Regulatory Submissions: Human Factors – FDA’s New and Renewed Expectations About this Webinar Now Available to View Online
March 21st, 2016
UL’s Mark Leimbeck speaks about risk management at recent MedTech Intelligence conference
February 24th, 2016
UL and MasterControl webinar “FDA Just Left! Now What?” now available to view online