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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
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
State of eConsent 2017 Report
INFOGRAPHIC: 14 Drivers of eConsent Adoption in Clinical Trials
The Essential Guide to Electronic Informed Consent
3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent
Reducing Regulatory Risk with eConsent
How eConsent Improves Consent Development
Recruiting and Retaining Patients with eConsent
3 Ways Electronic Informed Consent Benefits Trial Participants