Many of our clients and colleagues in the medical device community, driven to help patients and the medical provider community in this challenging time, want to pursue FDA’s Covid-19 Emergency Use Authorization (EUA) to do so.

If you’re a medical device manufacturer or supplier and have taken a look at FDA guidance for Covid-19 EUA and are a little confused or uncertain on the course of action to ensure medical device quality assurance, you’re not alone. That’s why Cannon Quality Group is pleased to announce a new series of infographics to help simplify the process and increase the medical device industry understanding of current FDA guidance and enforcement of the Covid-19 Emergency Use Authorization process.

The second of the 6-part series is focused on FDA guidance regarding Covid-19 EUA for face masks and respirators, and later installments in the series will cover digital health devices, remote patient monitoring, and telethermographic systems.

Sign up to receive all 6 of the medical device quality management infographics in the series. Please select “Covid-19 EUA Infographics” from the pull down menu. Request a FREE consultation with us by indicating so in the “How can we help you?” box.