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.

• 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