- TypeWebinar
- Location Aurora, Colorado, United States
- Date 10-10-2018
Education/Teaching/Training/Development
Business Development
Biotechnology
Medical/Healthcare/Hospital
OTHERS
OVERVIEW
This webinar will explain how to determine if your app is a medical device and if it will be subject to FDA cybersecurity requirements. The FDA approval process for mobile apps will be explained including FDA software validation requirements which are more extensive than just testing performance.
WHY SHOULD YOU ATTEND
The FDA Guidance explains how they intend to apply their regulatory authority to software applications intended for mobile medical apps. 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.
AREAS COVERED
LEARNING OBJECTIVES
Learn about FDA regulated mobile apps, along with FDA software validation requirements. Cybersecurity for mobile apps is very important. The FDA requirements for cybersecurity in the app design will also be explained in the webinar.
WHO WILL BENEFIT
For more detail please click on this below link:
Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882
Learn about the FDA regulated mobile medical apps along with FDA software validation requirements. The webinar also explains the significance of cybersecurity for mobile apps.