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Mobile Medical Apps (is it a FDA regulated device) and Cybersecurity
Tuesday, June 5th at 1:00pm EST
Online sale ends: 06/05/18 at 12:45pm EST
Online Event
Bethesda, MD 20817
-= series =-
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Talent

Edwin Waldbusser

Description
    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.

 

Objective :

 

  • ·         What mobile apps are medical devices
  • ·         What mobile apps will be regulated by FDA
  • ·         How to get a mobile app approved by FDA
  • ·         Cybersecurity for mobile apps explained

 

Why :

 

    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.

 

Areas Covered in the Session :

 

  • ·         What mobile apps are medical devices
  • ·         What mobile apps will be regulated by FDA
  • ·         How to get a mobile app approved by FDA
  • ·         Cybersecurity for mobile apps explained

 

Who Will Benefit:

 

  • ·         Development Engineers
  • ·         Production Management
  • ·         QA/ QC personnel
  • ·         Software developers
  • ·         IT personnel
  • ·         Legal dept

 

About Speaker:

 

    Edwin Waldbusser retired from industry after 20 years in management of development of medical device products and development of company Quality Systems. Products included IVD devices, kidney dialysis systems and inhalation devices. QS experience includes design control, risk analysis, CAPA, software validation, supplier qualification/ control and manufacturing/ non-conforming product programs.

 

    Edwin Waldbusser has a B.S. Mechanical Engineering from NYU and a M.B.A from Drexel University. He is certified by Lloyds of London as an ISO 9000 Lead Auditor and is a member of the Thomson Reuters Expert Witness network. He has 5 issued patents.

 

Event URL: https://www.compliancetrainingpanel.com/Webinar/Topic?WB=MD00098

 

 

Organizer: Compliance Training Panel

Website: www.compliancetrainingpanel.com/Webinar/Live

Contact: support@compliancetrainingpanel.com

Phone: 844-216-5230


Presented By

1:00pm to 2:00pm
Doors open at 1:00pm

General Admission: $229.00

Age
21+

Online Event<br> Bethesda, 20817

200

844-216-5230

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