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Impacting People's Lives

"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.

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Harness the power to transform clinical development

Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.

Research & Development Overview
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Real World Evidence. Real Confidence. Real Results.

Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.

REAL WORLD EVIDENCE OVERVIEW
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See markets more clearly. Opportunities more often.

Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.

COMMERCIALIZATION OVERVIEW
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Service driven. Tech-enabled. Integrated compliance.

Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.

COMPLIANCE OVERVIEW
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Intelligence that transforms life sciences end-to-end.

When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.

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Explore our library of insights, thought leadership, and the latest topics & trends in healthcare.

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THE IQVIA INSTITUTE

An in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.

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INSTITUTE REPORT

"Global Trends in R&D 2025

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EMEA Insights

"IQVIA thought leadership with a focus on EMEA.

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WHITE PAPER

"DCTs Deliver Big ROI

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WHITE PAPER

"Capturing value at scale: The $4 billion RWE imperative

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FEATURED INNOVATIONS
  • IQVIA Connected Intelligence™
  • IQVIA Healthcare-grade AI®
  • Human Data Science Cloud
  • IQVIA Innovation Hub
  • Decentralized Trials
  • Patient Experience Solutions with Apple devices
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Unlock your potential to drive healthcare forward

By making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.

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IQVIA AI is Healthcare-grade AI

Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.

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Your healthcare data deserves more than just a cloud.

The IQVIA Human Data Science Cloud is our unique capability designed to enable healthcare-grade analytics, tools, and data management solutions to deliver fit-for-purpose global data at scale.

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Innovations make an impact when bold ideas meet powerful partnerships

The IQVIA Innovation Hub connects start-ups with the extensive IQVIA network of assets, resources, clients, and partners. Together, we can help lead the future of healthcare with the extensive IQVIA network of assets, resources, clients, and partners.

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Proven, faster DCT solutions

IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.

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IQVIA Patient Experience Solutions with Apple devices

Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm.

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"At IQVIA your potential has no limits. We thrive on bold ideas and fearless innovation. Join us in reimagining what’s possible.

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Complete Consent

The proven, global eConsent platform

IQVIA Complete Consent is the user-friendly, flexible, and feature-rich electronic informed consent solution built to support diverse protocols at a global scale.

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Solutions IQVIA Technologies Orchestrated Clinical Trials Patient Engagement Suite Complete Consent

Deliver highly engaging compliant eConsent

Verified through more than 350 studies with over 400,000 participants and 10,000 sites, IQVIA Complete Consent meets the needs of all trial types.

eConsent helps sponsors achieve better outcomes across the entire study lifecycle, while delivering an enhanced experience for patients and more convenience for sites.

DEPLOY COMPLETE CONSENT AROUND THE WORLD WITH CONFIDENCE
IQVIA Complete Consent
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    IQVIA Complete Consent delivers unmatched value to all stakeholders

    Sponsors

    • Compliant data by reducing consent-related protocol deviations
    • Global delivery with configurable documents and multiple language support
    • Increase patient recruitment and retention to accelerate trial conduct
    • Deep experience in oncology, vaccines, cardiovascular, and more therapeutic areas
    • Consent reporting and analytics for study design and enrollment strategies

    Sites

    • Consenting workflows from the first document through amendments
    • Reduce administrative burden and errors compared to paper processes
    • Single sign-on and integrations to eliminate redundant data entry
    • Empower site staff to focus on patient experience and answer questions
    • Flexibility in document collections and version management

    Participants

    • Interactive multimedia features explain details of study participation
    • Make informed decisions about trial expectations, risks, and benefits
    • Review and sign digital consent forms on any internet enabled device
    • Accessible, configurable technology for pediatric, elderly, and impaired patients
    • Participants may highlight areas of the document for further discussion with the study physician

    Reduce protocol deviations

    In a review of nearly 100 trials across IQVIA that used eConsent, compared to paper, consent-related major and critical protocol deviations were reduced from an average of 14% to only 6%. This entailed a combination of electronic signature and print-to-sign modalities.

    SEE HOW

    Insight brief

    Deliver interactive, compliant remote consent

    The right remote consent solution provides participants with tools to understand the study and pose questions to site personnel, while minimizing disruptions to their daily lives. An eConsent solution should also empower study teams and sites to spend more time conducting the study by reducing the burden of administrative tasks such as addressing deviations.

    read now

    Insight brief

    IQVIA experts tailor eConsent for each study

    IQVIA Complete Consent supports all trial types and business models, from decentralized to traditional site-based trials, from standalone self-managed to full-service solutions with implementation services. We partner with sponsors at every step so you can deliver eConsent at sites around the world with confidence.

    learn more

    ECONSENT BROCHURE

    Transform the eConsent experience

    Discover how IQVIA Complete Consent delivers an accessible solution to patients, operational efficiencies to sites, and a powerful platform to sponsors implementing eConsent flexibly and compliantly around the world.

    download now

    OUR LATEST THINKING

    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
    Blog
    Stop Papering Over Consent Problems: Leverage eConsent for Clinical Trial Participants
    By: Vinita Navadgi

    Part 1: How eConsent Improves the Trial Experience for Patients and Sites

    Livre Blanc
    eConsent for Complex Clinical Trials

    How to deliver highly engaging informed consent for better study outcomes
    Webinar
    eConsent for Complex Trials Webinar
    Blog
    eConsent: the missing ingredient to more engaging clinical trials
    By: Vinita Navadgi

    Electronic consent products set the stage for a better trial experience for all stakeholders, but many sites and sponsors are wary of giving up their paper-based past.
    Fact Sheet
    IQVIA Integrated Complete Consent IRT eCOA

    Interoperable technology that improves data quality and usability while optimizing trial conduct
    Blog
    Biosample tracking: A consenting dilemma
    By: Sonia Fischer

    Don’t let vague consent forms prevent you from (re)using valuable specimens
    Blog
    Five Steps Up the Ladder to Higher Electronic Consent Adoption
    By: Kate Godwin-Smith
    Livre Blanc
    Going Global with eConsent
    Brochure
    IQVIA Complete Consent

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

    Product Resources

    Related Solutions

    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.

    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.

    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.

    Contact Us