FDA guidance to using eConsent in clinical trials
March 28, 2019 • Webinar 2 pm ETRegister
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