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Monitoring Considerations for Clinical Trials with eConsent
During this webinar, informed consent experts with decades of hands-on monitoring experience discuss the challenges they’ve encountered and how to overcome them with the integration of eConsent.

eConsent University Podcast: Episode 1
Jackie Brusch and Sam Sather discuss the various and changing regulations and guidances for eConsent, highlighting pre-implementation considerations and resources for clinical trial professionals.

Tips for Implementing an eConsent Solution
Industry expert Sandra "SAM" Sather shares her knowledge of how to properly implement an eConsent solution.

Translations and eConsent
When designing an informed consent, it's extremely important to consider the participants using it. Specifically, the consent should be created in a language that its primary audience will understand.

Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites
In this webinar, CRF Health's Sandra "SAM" Sather is joined by Giga Smith from Coastal Carolina Healthcare (CCHC) to discuss Electronic Informed Consent (eConsent) from the research site perspective.

Using eConsent in Clinical Research to Support Patient Understanding and Welfare