Elizabeth Pugh, Emergo MDR expert


Senior Consultant, Regulatory Affairs

Elizabeth Pugh has been a consultant with Emergo by UL since 2011 and has over 14 years of industry experience, primarily focused on orthopedic devices, including implantable devices. Elizabeth’s background includes: CERs, global vigilance reporting, 510(k) clearances, EU Technical Files, participating in risk management files, global regulatory strategy, and performing international regulatory research. As a Regulatory Affairs Consultant, Elizabeth manages Emergo by UL's vigilance activities in the EU, US, Australia, Singapore, Malaysia, and other markets. In this role, she has reviewed and submitted over 5,000 vigilance reports. Additionally, Elizabeth utilizes her regulatory background to complete a wide range of projects for clients such as technical file compilation, clinical evaluation reports, 510(k)s, regulatory research, and regulatory strategy reports. Prior to Emergo by UL, Elizabeth held RA positions at Stryker, ev3, and DJO Surgical.