A global pharma sponsor partnered with IQVIA Patient Suite to integrate IRT and eConsent, overcoming digital adoption challenges and streamlining trial operations. Using a unified delivery team, the solution went live ahead of schedule, reduced start-up times, and simplified workflows with single login access and consolidated documentation. Patients benefited from interactive consent, better understanding, and reduced burden, while sites gained consistent data, real-time consent notifications, and smoother training. The integration eliminated redundancy, improved compliance, and enhanced efficiency across reporting, data management, and stakeholder alignment, setting a new standard for digital trial execution.

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