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MOBILE HEALTH: MANAGING THE PROCESS TO REALIZE THE BENEFITS
Speakers
If you missed our webinar on mobile health device regulation for clinical trials, it’s not too late to hear about the opportunities to manage device validation and the  regulatory process to realize the benefits to your mobile health-enabled clinical trials. 
  • Understand why there is friction between consumer devices and traditional medical devices relative to development and marketing.
  • Understand the nature and scope of changes related to regulation of mHealth devices.
  • Understand the somewhat hidden costs to be managed in order to support a successful mHealth device.
A recording is now available to view online or share with 
colleagues - learn about the scope of changes in mobile health device regulation and the considerations for validating your device.

William Hanlon, PhD
Vice President, Head of Global Regulatory Affairs, Covance
REALIZE THE PROMISE AND POTENTIAL OF MOBILE HEALTH
Scott Thiel, MBA, MT (ASCP), RAC
Associate Director, Navigant Consulting, Inc.
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