Reduce Barriers, Get Clinical Trials Off the Ground Faster with eConsent
Custom content for Medrio by BioPharma Dive's Brand Studio
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
Fred Martin Vice President
Engineering & Product Management,
Megan Doerr, MS, LGC Principal Scientist
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