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Get to Know TrialConsent - Signant Health
TrialConsent offers a collaborative platform for developing and updating consent documentation and a real-time monitoring tool to track progress.
Signant Health Unveils its full Conference Line-up for SCOPE 2020
Subject matter experts, technologists, scientists and executives to advance patient-centric conversations with innovative clinical operations leaders from global pharmaceutical companies.
Signant Health finds growing eConsent adoption forecasts and the importance of eClinical integration in latest “State of eConsent” survey
Signant Health released the findings from its latest “State of eConsent” report, highlighting the sentiments, successes, and challenges of electronic informed consent practitioners around the world.
Delving into eConsent: Industry Survey Reinforces Patient Centricity
Signant conducted an electronic informed consent (eConsent) survey to obtain insights from sponsors and CROs. Here are the findings from this key piece of research
TrialConsent Self-Service and its Enablement
TrialConsent® Self-Service allows you to develop your own consent forms and documentation, create libraries for easy re-use across studies and maintain full control over your processes.
The University of Bristol Selects Signant Health's TrialConsent Solution in Oncology Trial
The Prestigious UK Academic Institution selected TrialConsent® to Administer eConsent to Benefit Sites and Patients in Future Clinical Research.
Signant Selected as eConsent Provider by Shanghai Mental Health Center
Signant Health has been selected to provide eConsent for a significant neuroscience study by the prestigious Shanghai Mental Health Center (SMHC).
The Essential Guide to Electronic Informed Consent
TrialConsent for IRBs and ECs (Ethics Committees)
Discover the value of TrialConsent (eConsent) for IRBs and Ethics Committees by Signant Health.
14 Drivers of eConsent Adoption
Signant Health CRO Partner Program
Become a CRO partner today. Sponsors what to know what your competitive edge is, so let's show them. We'll make sure you are distinguished and trusted for delivering across the Signant portfolio.
Enabling Electronic Informed Consent for Clinical Research Sites
Watch this information session on electronic informed consent designed exclusively for clinical research sites to see first-hand how eConsent can improve your informed consent process.
eConsent in Action - How It Works and Why Patients Appreciate It
In this 45-minute webinar on demand we discuss benefits for patients, sites and study teams, address common questions, and present a brief demo to help you make eConsent decisions for your trials.
Optimizing eConsent for Patient Centricity
Experts from across the clinical trial industry share their data, real case studies and expertise on how to best support patient centricity through eConsent.
CRF Health Looks To Simplify eConsent For Both The Patient And The Researcher
Clinical Informatics News and Rauha Tulkki-Wilke discuss eConsent adoption & how TrialConsent bypasses the eConsent setup hurdle for sponsors while delivering a patient-centered, easy-to-use solution.
The Top 10 Myths of Electronic Informed Consent
The top 10 myths about electronic informed consent (eConsent) and the journey that makes "going electronic" the only path for industry leaders.
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.
Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption
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
eConsent: Five (5) Key Areas of Preparation