Going “E” With Informed Consent for Clinical Trials
Product Details
Then read on…
As consent forms get longer and more complex, participant enrollment and retention rates fall.
Innovative pharma/device sponsors and CROs have started making consent forms more visual, not just lines of text.
This encore presentation will give attendees straightforward advice and guidance. Attendees will learn the benefits of e-consenting, which include:
- How a more visual format overcomes language and literacy barriers
- Why electronic consent makes data gathering and remote monitoring easier on sponsors and subjects
- How version control and audit trails are easier to maintain and reduces the risk of non-compliance
- Why e-consenting speeds up trial enrollment and gets products to market faster
Join clinical trial specialists Dr. Susan Brink and Sherri Bracy in this 90-minute encore presentation, as they answer these questions:
- What should you ask your IRB when initiating e-consent — how will they view the process and will it affect trial approval and monitoring?
- How does a site/CRO or sponsor determine which e-consent application is the best fit for their organization?
- What are the features that every e-consent application must have (e.g., revision control, audit trails)?
- Tips and tricks for monitoring and auditing e-consents
- Tales from the trenches — what are some of the common impacts an e-system has on the IRB process?
You and your colleagues will participate from the comfort of your own office, conference room or auditorium. No planes, no hotels, no precious time away from work and family — just 90 minutes of solid, interactive learning via the Web.
And here’s more good news: Your entire team can participate at no extra cost. One low fee covers every participant at your location. It’s easy to add more locations, too, at bargain rates. Simply call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally to learn about multisite discounts.