White Paper

Data on the go: Mobile Application Considerations for Clinical Trials and Beyond 

What are the necessary regulatory and ethical considerations when utilizing an app or connected device in human subjects research?

Our comprehensive guide is essential for those utilizing apps in clinical trials, covering topics like:

  • How medical device regulations apply (or don’t) to mobile apps and connected devices
  • How to evaluate apps for research
  • Considerations for participants and study staff
  • What IRBs look for when reviewing research involving apps
  • Consent language regarding app privacy policies and Terms of Use
  • Additional resources to support app and device development 

Download our free white paper.

Who Should Watch?

CEU Credits

Certificate of Attendance

Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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