Home » Process Improvement » eConsent: Five (5) Key Areas of Preparation

× Share this Article

Facebook
Twitter
Email
LinkedIn
Google+

eConsent: Five (5) Key Areas of Preparation

April 2, 2018 Jackie Brusch

Share this Article
Facebook
Twitter
Email
LinkedIn
Google+

As seen in InSite, the Global Journal for Clinical Research Sites via the Society of Clinical Research Professionals

eConsent: Five (5) Key Areas of Preparation from CRF Health

About the Author

Jackie Brusch is the Content Marketing Manager at CRF Health.

Previous Video

The Value of Electronic Informed Consent

In Pursuit of eConsent: Best Practice Recommendations for Successful Integration

Provided by The Journal for Clinical Studies - Original at https://issuu.com/mark123/docs/jcs_volume_9_2_we...

Other content in this Stream

Successful Adoption of eConsent Best Practices for Integrating eConsent Technology

Read

eConsent Myth #4: eConsent is not used and won't be accepted outside of the United States

2:59

How eConsent Improves Consent Development

Watch

1:01:36

Monitoring Clinical Trials with Electronic Informed Consent

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.

Watch

34:36

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.

Watch

The Essential Guide to Electronic Informed Consent

Read

3:05

Tips for Implementing an eConsent Solution

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

Watch

State of eConsent 2017 Report

Read