July 21st, 2017

PRE-RECORDED WEBINAR: Business Impact of the new EU Medical Device Regulation – An Executive Briefing

The UL Health Sciences team is pleased to welcome Dr. Itoro Udofia to UL as our new Head of Notified Body. We are excited to be able to share the 20 years of experience and knowledge to our customers that he brings to UL. On Thursday, July 20th, 2017 Dr. Udofia presented a live webinar… read more

July 4th, 2017

PRE-RECORDED WEBINAR: Meeting new FDA Expectations for ISO 18562 VOC and Particle Testing for Medical Devices

US FDA 510(k) submissions must include data regarding biocompatibility of any patient contacting materials (directly or indirectly) on all medical devices. For respiratory and ventilation devices, a key component of the biocompatibility evaluation is measuring chemicals and particles that may be released into the breathing gas pathway. Until recently, only general guidance was provided to… read more

July 4th, 2017

PRE-RECORDED WEBINAR: Medical Device Use Error – Root Cause Analysis

About this webinar: In this 60+ minute webinar, Michael Wiklund, Andrea Dwyer and Erin Davis, senior members of the UL Human Factors Engineering (HFE) practice described the regulatory and commercial imperative to identify the most likely root causes of medical device use errors. In this recording, they reflect on the harm that arises from use… read more

June 7th, 2017
Cybersecurity Task Force Recommendations hit Congress
March 27th, 2017
UL Principal Engineer Pamela Gwynn quoted in ODT article.
March 3rd, 2017
Safety Standards: Making India’s Healthcare Sector Safer and Future Ready!
January 5th, 2017
What to look for in a Notified Body
October 24th, 2016
UL Northbrook expands CBTL scope with 3 additional IEC 60601 Medical Particular Standards for use with IEC 60601
October 14th, 2016
PRE-RECORDED WEBINAR: Business Impact of the new EU IVD Regulation – An Executive Brief with Sue Spencer
October 13th, 2016
PRE-RECORDED WEBINAR: Validation needs for packages of medical devices