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hello and thanks for joining us on our final day of the green light guru true quality summit I hope you've had a chance to enjoy the last few days of learning actionable tips trends and best practices to achieve true quality for your medical devices and business this session is on how to get your Kovan 19 related medical device to market under FDA's emergency use authorization eua I'm Jessica Lyons senior medical device guru here at green light guru and I will be monitoring I will be moderating for this special session I know our speaker Kyle Rose is really looking forward to sharing his experience working with manufacturers and distributors around the world to get to Kovan 19 related medical devices to market under FDA's eua before we dive too deep into today's session and introduce our speaker and his company rook quality systems I'm gonna touch on a few items really quickly first this is going to run for about 45 minutes in total and will include a Q&A session at the end where Kyle is going to answer all of your questions for as many as we can get to in that time so I encourage you to submit your questions throughout the presentation as they come up in the box on the right-hand side anything that we are unable to answer Kyle will be able to follow up with you guys after the session and this entire session will be recorded once this session wraps up there is about a 10 minute break before the next live session begins if you're interested in learning about why remote research is or isn't right for your project make sure you're registered for the next session and use your unique link to tune in if you aren't already signed up you can still register at virtua - summit green light guru now Before we jump in I'd like to share a few words about green light guru and why we put on this free virtual summit if you've been on one of our training sessions before then you know we put these on because improving the quality of life is our mission here at green light guru likely a similar mission as many of you at today's summit anything we can do as an organization that helps device makers bring safer life-changing devices to market quicker and with less risk aligns with that mission we are constantly looking for will ways to fulfill that mission whether it's through hosting free events and training sessions through partnering with world-class medical device consultants or through our award-winning medical device QMS software if you'd like to learn more about why medical device companies from across the globe are moving away from paper-based general-purpose quality management systems and adopting our purpose-built medical device quality management software I encourage you to head on over to .amazingpublicspeaking.com works as a quality system advisor for multiple medical device companies overseeing overall quality strategy and ensuring compliance through documentation and auditing services Kile encourages the simplification of quality systems to...