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Do you need medical device compliance guidance for FDA Covid-19 Emergency Use Authorization (EUA) products?
June 2, 2020

Do you need medical device compliance guidance for FDA Emergency Use Authorization (EUA) products?Are you a little confused or uncertain on the course of action to ensure medical device quality assurance for FDA Covid-19 Emergency Use Authorization (EUA)? Need some guidance for Covid-19 EUA? You’re not alone. 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 EUA process.

Get your complimentary medical device compliance guidance infographics, a 6-part series or simply request one in your area of product development from the options below. Make your request by June 15th to also receive your courtesy consultation.

FDA compliance guidance Covid-19 EUA infographics include the following:

  • Ventilators
  • Face masks & Respirators
  • Non-invasive remote patient monitoring devices
  • Digital health devices (DHDs) for treating psychiatric disorders
  • Telethermographic systems, and
  • Remote ophthalmic devices

Please select “Covid-19 EUA Infographics” from the pull down menu. Request your FREE consultation with us by indicating so in the “How can we help you?” box.

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