Our Medical Device and Technology team has been at the forefront of the COVID-19 legal response since the pandemic swept across the globe. In just a few short months, our team has taken on nearly 200 matters, ranging from attaining U.S. Food and Drug Administration (FDA) Emergency Use Authorizations (EUAs) for critical medical devices and testing kits, to advising on legal risks of producing various types of personal protective equipment (PPE) and importing devices – such as ventilators from China – for use in the U.S. and around the world.