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MAIN/Solutions
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SOLUTIONS
  • Research & Development
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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
Research & Development Quick Links
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
Technology Quick Links
MAIN/Products
Products/
CLINICAL PRODUCTS
COMMERCIAL PRODUCTS
COMPLIANCE, SAFETY, REG PRODUCTS
REAL WORLD PRODUCTS

CASE STUDY

"Data in a Day

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MAIN/Insights
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

"Global Trends in R&D 2024

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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 powered by Apple
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 powered by Apple

Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm. IQVIA and Apple are collaborating to bring this exciting future of personalized care directly to devices patients already have and use.

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MAIN/Careers
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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MAIN/Contact Us
Contact Us/
IQVIA RIM SMART CONTENT MANAGEMENT

Orchestrate submission-ready regulatory content at scale.

Empower your regulatory teams to collaboratively plan, author, review and approve compliant documents.

CONTACT US
Solutions Safety & Regulatory Compliance Regulatory Compliance IQVIA RIM Smart Content Management

Successful regulatory content management starts here

IQVIA RIM Smart Content Management is an essential part of the RIM Smart platform for regulatory information management, providing a versatile SaaS solution to assemble augmented submission content for publishing.

Build and track authoritative submission content that is GXP-compliant and in accordance with industry standard CTD and eCTD content structures.

Enhance document quality with intuitive collaborative tools

Put an end to using siloed legacy systems, file shares, and email attachments for regulatory document generation. RIM Smart Content Management makes it easy for teams to work together on submission content – both in real-time and asynchronously.

More than 340 pre-formatted, global authoring templates, with automated insertion of pre-configured custom properties into new documents.

Predefine or create new document views, name and share views and modify by adding and removing criteria easily.

Improve document production through better collaboration and transparency among regulatory stakeholders.

Intuitive dashboard displays user activities including active documents, workflows, tasks, and notifications in a single location.

Pre-built and configurable, task-driven workflows for versioning, review, and approval of document submissions in a GXP-compliant fashion.

Real-time oversight for workflow owners

Provide pharmaceutical organizations with peace of mind through a superior solution that reduces risk, cost, and delays in submission content workloads.

  • Trust that all stakeholders are planning, authoring, reviewing, and approving one authoritative document.
  • Synchronize full product metadata including regional market and study information.
  • Gain real-time traceability about document contributors, task completion, and overall timeline.
  • Ensure regulatory readiness with support for FDA’s 21 CFR Part 11 requirements.

FACT SHEET

IQVIA RIM Smart Content Management

Discover how IQVIA RIM Smart Content Management streamlines regulatory workloads, enabling teams to accelerate approvals and bring breakthrough treatments to patients faster.

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OUR LATEST THINKING

BLOG
Innovating Regulatory Services: Benefits of End-to-end Regulatory Labeling Revamp

WHITE PAPER
eCTD 4.0 Implementation: Including Understanding of Regional Differences and Benefits

FACT SHEET
IQVIA RIM Smart: Regulatory Information Management   

WEBINAR
The Future of Documents: Structured content and integrated data

Related solutions

RIM Smart Labeling

Leverage a global network of Phase I clinical pharmacology units to build diversity in patient populations and access a range of geographic regions for early clinical development (ECD) programs.

IQVIA Regulatory Productivity Tools

Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.

Regulatory Intelligence

Strengthen your portfolio by making more informed decisions and fewer assumptions, and prepare for the impact of new research discoveries and events.

Contact Us