Implementing e-Consent for Clinical Trials

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Implementing e-Consent
for Clinical Trials

The simple fact about electronic informed consent is that it's much more than a digital handwritten signature.
 

This management report covers the major benefits of employing e-consent software and answers your toughest questions about it, including:
 

  • How to determine which software is right for your company

  • How to keep a site-wide system fully compliant as regulations change

  • How to determine how much training your staff will need to use the new software

  • How electronic media help keep patients better informed

  • How much is too much — or too little — to spend on an e-consent system

Implementing e-Consent for Clinical Trials will provide you with checklists and guides that will help you make an informed decision about the software that's best for you, as well as prepare you to talk to prospective vendors:
 

  1. A 5-step overview of the e-consent process

  2. 7 questions you should ask the provider of an e-consent application

  3. A step-by-step workflow for e-consent development

  4. 4 pillars of successful e-consent implementation

Changing over to an e-consent system is probably not far away in your future. Order your copy of Implementing e-Consent for Clinical Trials today.

 

PDF Edition

Available Format

PDF Edition — $397

Table of Contents

  • Introduction
  • Informed Consent and the E-Consent System
  • The e-Consent Process: A Case Study
  • Regulatory Compliance
  • And More ...

View the entire TOC

Who Will Benefit

  • Compliance officials
  • QA/QC personnel
  • Regulatory affairs professionals
  • Training personnel
  • Procedural document writers
  • Clinical operations personnel
  • Clinical investigators
  • Clinical research coordinators

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