.svg){kind=icon}
Complete Consent
IQVIA Complete Consent is the user-friendly, flexible, and feature-rich electronic informed consent solution built to support diverse protocols at a global scale
Article
From Signatures to Success: How Digital Consent Accelerates Trials, Enhances Compliance, and Engages Patients
Jun 11, 2025
This article explores how digital informed consent is revolutionizing clinical trials by replacing outdated paper-based processes. It highlights the benefits of digital consent, including faster study start-up, improved regulatory compliance, reduced administrative burden, and enhanced patient and site engagement. The piece by Vinita Navadgi also emphasizes how digital tools support both operational efficiency and patient-centric trial design.
You may also be interested in
Insight Brief
Why not Paper? Answering Five Common eConsent Questions
Blog
Stop Papering Over Consent Problems: Address Them Head-On with eConsent
Part 2: How eConsent delivers value for sponsors
Brochure
IQVIA Complete Consent
Deliver eConsent to sites and study participants around the globe with confidence
Related solutions
Interactive Response Technology
Power your decentralized trial with an agile randomization and trial supply management solution that supports supply flexibility and optimization as well as adaptable direct to patient options.
eCOA
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.
IRT eCOA
Improve study quality, accelerate decision making and reduce site and sponsor burden by harnessing the power of IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution.