Date(s) - 03/06/2019
1:00 pm - 2:00 pm
This webinar will explain how to determine if your mobile apps are medical devices and if they will be subject to FDA requirements. The FDA approval process for mobile medical apps 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 cybersecurity requirements in the app design will also be explained.
WHY SHOULD YOU 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 mobile apps they consider a medical device.
Apps that are medical devices must meet all FDA software validation requirements and FDA cybersecurity 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.
- What mobile apps are medical devices?
- Which mobile apps are regulated by FDA?
- How to get mobile medical apps approved by FDA
- Cybersecurity for mobile apps explained
Learn about mobile medical apps, including FDA software validation requirements and FDA cybersecurity requirements.
WHO WILL BENEFIT
- Development Engineers
- Production Management
- QA/ QC personnel
- Software developers
- IT personnel
- Legal Department
To Register (or) for more details please click on this below link:
Toll Free: +1-888-300-8494