Live webinar on FDA Regulation of Mobile Medical Apps By compliance2go October 17, 2012

Why should you Attend:

The number of mobile applications or “apps”, including mobile medical apps, is ever increasing and an undeniable mainstay of medicine moving forward. Anyone planning to enter the mobile medical apps field who plans to market their apps in the U.S. must understand FDA’s plans for regulating mobile medical apps moving forward. Moreover, as FDA’s plans are not yet completely finalized, it is also an opportunity to understand what FDA is planning to do and attempt to impact the process.

Webinar Includes:

Q/A Session with the Expert to ask your question

PDF print only copy of PowerPoint slides

60 Minutes Live Presentation

Description of the Topic:

On July 21, 2011, FDA issued its draft guidance for the regulation of mobile medical apps. The seminar will summarize FDA’s current plans for regulating mobile medical applications, as described in the draft guidance. It will also explore the practical implications of FDA’s regulatory plans for mobile medical apps manufacturers and marketers, including those firms which provide the mobile platforms on which the “apps” are used. It will also discuss and update attendees on recent Congressional action on mobile medical apps and how the activity affects FDA’s plans.

Who will benefit:

Representatives of manufacturers and marketers of mobile medical applications and mobile platforms as well as other medical devices, including in-house counsel, outside FDA counsel, regulatory affairs personnel, and regulatory consultants

Official Website: https://compliance2go.com/index.php?option=com_training&speakerkey=39&productKey=141