Reduce Barriers, Get Clinical Trials Off the Ground Faster with eConsent

Custom content for Medrio by BioPharma Dive's Brand Studio

LIVE WEBINAR
Thursday, March 28th | 2 pm EST

Duration: 1 hour
Can't make the live date? Register and we'll send you a link to the recording. ​


​eConsent has numerous benefits for patients – it’s convenient, and it allows them to begin the process, take a break and pick up where they left off. It also allows patients to stay more informed during the trial process.

Even better, those benefits to patients translate to positive outcomes for the clinical trials themselves. eConsent can lead to improved compliance, higher patient enrollment and patient retention.

In this webinar, we will address:

  • The challenges and risks of using a paper-based consent system
  • The benefits – for both patients and companies – of using eConsent
  • Where the eConsent market is headed
  • Insight on FDA guidance

SPEAKER  

Fred Martin
Vice President
Engineering & Product Management,
Medrio


Megan Doerr, MS, LGC
Principal Scientist
Governance,
Sage Bionetworks

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