Mobile medical apps(is it a FDA regulated device) and cybersecurity

Website https://bit.ly/2CTmKhI | Edit Freely

Category FDA software validation requirements;FDA cybersecurity requirements; Mobile medical apps

Deadline: October 10, 2018 | Date: October 10, 2018

Venue/Country: Training Doyens 26468 E Walker Dr,Aurora, Colora, U.S.A

Updated: 2018-09-12 12:51:59 (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 FDAcybersecurity 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

• What mobile apps are medical devices?

• What areFDA regulated mobile apps?

• How to get a mobile app approved by FDA?

• Cybersecurity for mobile apps explained

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

• Development Engineers

• Production Management

• QA/ QC personnel

• Software developers

• IT personnel

• Legal dept

For more detail please click on this below link:

https://bit.ly/2MnI4vr

Email: supporttrainingdoyens.com

Toll Free: +1-888-300-8494

Tel: +1-720-996-1616

Fax: +1-888-909-1882