By Kate Godwin-Smith, Director, Client Services, Patient Consent Solutions, IQVIA Technologies
When it comes to gaining the benefits of electronic consent (eConsent) in clinical trials, site adoption is the key. When a sponsor provides an eConsent solution to sites, they are enhancing the very important conversation that must take place between investigator and clinical trial participant, translating the protocol into patient-friendly language and learning modalities that help participants understand their obligations. Explore the steps up the ladder of eConsent adoption and reach new heights with every study.
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