June 10, 2020
Manufacturing after COVID-19: Prepare Your Medical Devices for Post-EUA World
Regulatory agencies from around the world are fast-tracking regulatory approvals for medical devices, but what happens when emergency use authorizations (EUAs) end?
Business Revitalization Efforts for Long-term Success
UL has developed a visual guide that explores some bold steps companies are taking in the midst of a pandemic to revitalize their businesses and ensure long-term sustainability in an uncertain world.
Webinar - COVID-19 Series: Reopening and Recover Depends on Safe Medical Devices
UL's VP & General Manager of Healthcare and Life Sciences, Upayan SenGupta and the founder of Plug and Play, Saeed Amindin on the importance of medical and diagnostic device safety for re-opening and recovery during a pandemic.
White Paper: ISO 10993-1 and Biocompatibility Requirements for Medical Devices
This UL white paper will provide an overview of the structure and requirements presented in the latest version of ISO 10993-1 and provide details on the biological safety evaluation process set forth in Annex B of the standard.