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.

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

Technology informed by unparalleled Decentralized Trials (DCT) operational experience and delivered at global scale.

Deliver eConsent to sites and study participants around the globe with confidence

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