HEALTHCARE TRAINING 2020 - Mobile Medical Apps(is it a FDA Regulated Device) and Cybersecurity

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Category HEALTHCARE TRAINING 2020

Deadline: November 10, 2020 | Date: November 10, 2020

Venue/Country: Online event, U.S.A

Updated: 2020-09-28 20:06:08 (GMT+9)

Call For Papers - CFP

This webinar will explain how to determine if your app is a medical device and if it will be subject to FDA requirements.

The FDA approval process for a new app will be explained including FDA requirements for software validation which are more extensive than just testing performance. Cybersecurity is very important for mobile apps. The FDA requirements for cybersecurity in the app design will be explained.

Why you should Attend: The FDA has released a Guidance explaining how they intend to apply their regulatory authority to software applications intended for use on mobile platforms. They have defined what types of apps they consider a medical device. Apps that are medical devices must meet all FDA device requirements, however, FDA will not enforce their requirements on Mobile apps that meet the FDA’s definition of a medical device but pose a low health risk.

This webinar will explain how to determine if your app is a medical device and if it will be subject to FDA requirements. The FDA approval process for a new app will be explained including FDA software validation requirements which are more extensive than just testing performance.

Cybersecurity is very important for mobile apps. The FDA requirements for cybersecurity in the app usage will be explained.