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The Essential Guide to Electronic Informed Consent

 

 

 

Informed consent is more than just a form – it's a process.

Regulators and industry groups are pushing for the adoption of electronic informed consent (eConsent) for the multitude of benefits it offer patients as well as sponsors and site teams, but the technology is so new, it can be hard to know where to start.

Download our latest eBook, "The Essential Guide to Electronic Informed Consent," to learn how eConsent enhances the consent process by: 

 

  • Streamlining the process for real-time access to patients/study teams 
  • Designing the electronic consent to support adult learning
  • Enhancing regulatory compliance to reduce risks
  • Saving sponsors time and money
  • ...And more!

 

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How Electronic Data Collection Helps Meet the FDA's Quality Guidelines
How Electronic Data Collection Helps Meet the FDA's Quality Guidelines

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FDA Supports Innovation in Clinical Trials with eConsent
FDA Supports Innovation in Clinical Trials with eConsent