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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