Originally featured in the Research Quality Association (RQA) magazine, Quasar, the quarterly member's magazine.
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eConsent University Podcast: Episode 1
Reducing Regulatory Risk with eConsent
Preparing for eConsent - A Step by Step Guide for Site Personnel
5 steps to help sites prepare for implementing an electronic informed consent (eConsent) solution.
eConsent: A Look Back at 2017 & Predictions for 2018
Mika and Jackie discuss the progression of eConsent in 2017 and predict where the industry is headed in 2018.
Best eConsent Resources of 2017
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.
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.
eConsent: Five (5) Key Areas of Preparation
CRF Health Launches TrialConsent™ 2.0 Platform
TrialConsent™, An Electronic Informed Consent Solution
eConsent: Enabling the Patient-Centered Clinical Trial of Tomorrow, Today
Can Seniors Use eConsent?
Electronic Informed Consent: 2017 Industry Survey Results
Sam Sather, Regulatory & Quality Lead for TrialConsent™, discusses survey findings from the State of eConsent 2017 Report. Find out why 82% of pharma companies are projected to adopt eConsent by 2020.
State of eConsent 2017 Report - Site Edition
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_web/58 For more information about electronic informed consent please visit www.crfhealth.com
Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption
Provided by ACRP's Clinical Researcher Magazine. Original at https://www.acrpnet.org/2017/04/01/recruitment-retention-breaking-barriers-econsent-adoption/ For more information on electronic informed
FDA Supports Innovation in Clinical Trials with eConsent
Visibility and Oversight: What Paper Informed Consent Isn't Offering You
Speakers from Chesapeake IRB and CRF Health discuss informed consent oversight and visibility. See how electronic informed consent (eConsent) enables top pharma companies achieve greater transparency.
State of eConsent 2017 Report
INFOGRAPHIC: 14 Drivers of eConsent Adoption in Clinical Trials
The Essential Guide to Electronic Informed Consent