Your Consent Process Can Make or Break Your Studies

Consent is an essential part of the patient journey. Yet, clinical research continues to struggle with achieving—and maintaining—informed consent throughout the course of a study. What can trial operators do to overcome challenges with health literacy, paper processes and consent workflows that are built for clinicians, not patients?

In this paper, we will explore:

  • The role consent plays in the success of your studies
  • How to identify and overcome barriers that impact informed consent
  • Achieving continuous informed consent with diverse patient populations
  • Unlocking patient-centricity in your trials with consent

We will also discuss how the industry is shifting towards greater adoption of eConsent to strengthen patient comprehension and preserve trial outcomes.



Field will not be visible to web visitor

Copyright 2021 Industry Dive | Privacy Policy | Terms of Use