Sr. Director, Product Management, AI and Technology Solutions, IQVIA Technologies
Director, Client Services Project Management, Patient & Site Delivery, IQVIA Technologies
Electronic consent (eConsent) systems have proven to add value to patients, sponsors, and sites. However, varying regulations across regions and countries can impact implementation of eConsent solutions and dilute the benefits. How can clinical trial professionals adapt a global approach to eConsent rollouts that accounts for these differences?
Join IQVIA Technologies for an informative webinar on electronic signature (eSignature) technology for eConsent. We’ll delve into global regulatory scenarios and options for meeting eSignature requirements in each scenario, including the benefits and limitations of:
Learn what to look for in eConsent solutions to ensure you’re prepared for every trial.
IQVIA Complete Consent is the user-friendly, flexible, and feature-rich electronic informed consent solution built to support diverse protocols at a global scale
Technology informed by unparalleled Decentralized Trials (DCT) operational experience and delivered at global scale.
Fast, flexible and proven, IQVIA’s industry-leading electronic clinical outcome assessment (eCOA) platform ramps up efficiencies, delivers real-time data, and sharpens insights through best-in-class technology and a better patient experience.
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