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Article
From Signatures to Success: How Digital Consent Accelerates Trials, Enhances Compliance, and Engages Patients
Jun 11, 2025
  • Library
  • From Signatures to Success: How Digital Consent Accelerates Trials, Enhances Compliance, and Engages Patients

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This article explores how digital informed consent is revolutionizing clinical trials by replacing outdated paper-based processes.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

Case Study
Integration of IRT and eConsent with Unified Delivery Provides Robust Solutions to Clinical Trial Sponsor
Insight Brief
Why not Paper? Answering Five Common eConsent Questions
Blog
Stop Papering Over Consent Problems: Address Them Head-On with eConsent
By: Vinita Navadgi

Part 2: How eConsent delivers value for sponsors
Brochure
IQVIA Complete Consent

Deliver eConsent to sites and study participants around the globe with confidence

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Complete Consent

Deliver eConsent to sites and study participants around the globe with confidence

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.

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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.

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