This fact sheet explains how IQVIA Complete Consent helps clinical trial sponsors meet complex global electronic signature requirements by supporting Qualified Electronic Signatures (QES) alongside Advanced Electronic Signatures (AES). Designed to comply with the EU eIDAS framework, QES provides the highest level of legal assurance through verified participant identities, certificate-based signatures, secure authentication, tamper protection, and comprehensive audit readiness. The platform integrates with Qualified Trust Service Providers (QTSPs) to automate identity verification and certificate generation while maintaining a seamless participant experience. By offering flexible signature options for decentralized, remote, high-risk, and multinational studies, IQVIA enables organizations t

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