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.