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SOLUTIONS
  • Research & Development
  • Real World Evidence
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  • Safety & Regulatory Compliance
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LIFE SCIENCE SEGMENTS
HEALTHCARE SEGMENTS
THERAPEUTIC AREAS

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
Real World Evidence Quick Links
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
Commercialization Quick Links
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
Safety & Regulatory Compliance Quick Links
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.

TECHNOLOGIES OVERVIEW
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MAIN/Products
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CLINICAL PRODUCTS
COMMERCIAL PRODUCTS
COMPLIANCE, SAFETY, REG PRODUCTS
REAL WORLD PRODUCTS

CASE STUDY

"Data in a Day

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Insights/
BLOGS, WHITE PAPERS & CASE STUDIES

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

DISCOVER INSIGHTS
THE IQVIA INSTITUTE

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

SEE LATEST REPORTS

INSTITUTE REPORT

"Digital Health Trends 2024 - Implications for Research and Patient Care

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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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MAIN/About
About/
FEATURED INNOVATIONS
  • IQVIA Connected Intelligence™
  • IQVIA Healthcare-grade AI™
  • Human Data Science Cloud
  • IQVIA Innovation Hub
  • Decentralized Trials
  • Patient Experience Solutions with Apple devices
WHO WE ARE
NEWS & RESOURCES

INVESTOR RELATIONS

"Visit our investor relations site for more information.

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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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Careers/
WORKING AT IQVIA

Our mission is to accelerate innovation for a healthier world. Together, we can solve customer challenges and improve patient lives.

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LIFE AT IQVIA

Careers, culture and everything in between. Find out what’s going on right here, right now.

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WE’RE HIRING

"Improving human health requires brave thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.

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IQVIA Regulatory Productivity Tools

Boost your regulatory productivity.

Today’s stringent, global regulatory environment is exacting. And staying in compliance is an on-going, time-consuming series of activities.  IQVIA

Productivity Tools make it easy to rapidly prepare, publish and validate eCTD and non-eCTD electronic submissions to regulatory authorities, giving your regulatory staff valuable time back for higher-level activities.

Get a 14 Day Free Trial. We'll have you setup within days!

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Solutions Safety & Regulatory Compliance Regulatory Compliance IQVIA Regulatory Productivity Tools
Try before you buy
Test drive before making a commitment. Access IQVIA Productivity Tools in a complimentary trial. Discover how they can simplify your regulatory staff’s daily activities, improving cycle times and minimizing risk.
Request a free trial

Improve your cycle times with IQVIA Regulatory Productivity Tools

Our research shows that ‘getting it right’ is a leading concern of regulatory professionals. IQVIA’s Productivity Tools make authoring and PDF publishing easy, fast and efficient. And our validation tool ensures that what you submit is in technical compliance with health authority requirements.

  • Prepare, publish, and validate eCTD and Non-eCTD e-submissions
  • Increase efficiency and reduce infrastructure development cost
  • Optimize cycle times with well-designed tools and intuitive interface

LEARN MORE ABOUT REGULATORY PRODUCTIVITY TOOLS

Adopt Technology Solutions to Innovate and Streamline Your Regulatory Services

Fact sheet
IQVIA RIM Smart Submission Management

FACT SHEET
IQVIA Regulatory Templates: Get it right the first time

FACT SHEET
IQVIA Regulatory PDF Tools: Simplify publishing and review

FACT SHEET
IQVIA eSubmission Validator: Verify submissions ahead of time

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Create the right new regulatory document every time

Select the right shell document for your regulatory work with IQVIA Regulatory Templates. Right down to the specific region, module and document type required.

  • Simple, menu-driven system provides quick start for regulatory authoring
  • Over 320 shell documents defined by regulatory agencies and the ICH (International Council for Harmonization)
  • Cover the marketing and clinical trial application processes for submission to EU’s EMA, U.S. FDA, Swissmedic and Health Canada
  • Includes regulatory-specific add-in for Microsoft® Office Word

Publish PDF files faster and easier

Specifically designed for the life sciences industry, IQVIA Regulatory PDF Tools provide customers with a simple, practical way to prepare PDF documents for submission.

  • Assists publishers and reviewers in preparing, publishing and delivering regulatory PDF documents
  • Addresses specific needs in accordance with regulatory agency and industry requirements.
  • Among fastest, most efficient PDF tools in the industry due to built-in intelligence and intuitive user interface

Assure technical compliance with regulatory agencies around the world

IQVIA eSubmission Validator verifies electronic Common Technical Documents (eCTD) and Non-eCTD Electronic Submissions (NeeS) documents, ensuring compliance with regional and ICH specifications and requirements prior to dispatch.

  • Validate compliance before submitting your document(s) to a specific agency, minimizing the risk of refusal to file or rejection due to technical issues
  • Receive a confidential report at the end of each validation
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Regulatory Compliance

Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.

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