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FDA Regulations on Mobile Apps and Medical Devices

When is an iPad no longer an iPad and instead considered a regulated medical device by the FDA? To help member institutions see this important distinction with more clarity, the GIR hosted Sharon R. Klein, JD, partner at Pepper Hamilton, LLP to explore how existing guidelines play into the larger picture of data privacy, patient care, and government regulations.

Watch a recording of this presentation.
This presentation was recorded on July 23, 2014 and is approximately 60 minutes in length.
Download the presentation slides. 

Additional Resources:

FDA Home on Mobile Medical Applications

Pepper Hamilton Client Alert - Hacking and Medical Devices 

Pepper Hamilton Client Alert - Mobile Devices and FDA Regulations 

Westlaw Journal Health Law - Telemedicine and Mobile Health 



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Upcoming and Recent Events

2018 GIR Leadership Institute
February 27-March 2, 2018
AAMC Learning Center
Washington, D.C.
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2018 Information Technology in Academic Medicine Conference
June 5-8, 2018
Westin Austin Downtown
Austin, Texas

2017 Learn Serve Lead: The AAMC Annual Meeting
November 3-7, 2017
Boston, Mass.

2017 GBA/GIP/GIR Joint Spring Meeting
May 9-12, 2017
Hyatt Regency Atlanta
Atlanta, Ga.
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