How to deliver highly engaging informed consent for better study outcomes

As clinical trial protocols become more complex, patient informed consent forms and processes become more complicated as well. Not only is it critical to effectively engage patients in the consenting process early to ensure protocol adherence and meet trial milestones, it’s essential that their consent be tracked from initial screening through cohort or treatment group assignment and each subsequent amendment.

A feature-rich electronic consent platform can provide an easy, secure way to deliver a highly engaging, regulatory compliant informed consent process that supports better study outcomes – especially in novel trial designs such as basket, umbrella, and platform trials.

In this webinar, IQVIA Complete Consent leaders will share how a robust eConsent solution can be customized to support these complex multi-stage studies and high-risk patient populations with an efficient customized, site- and participant-friendly consenting experience.

3 Key take-aways

Join IQVIA Technologies leaders to learn why eConsent is the ideal tool for:

• Consenting patients in complex trial designs, such as umbrella and bucket designs requiring numerous consents
• Trials across complex therapeutic areas and indications, including oncology, pediatrics, and emergency medical scenarios where patients may require a legal representative to provide consent on their behalf
• Supporting sites to accurately execute complex consenting workflows and tracking throughout a clinical trial