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MAIN/Solutions
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SOLUTIONS
  • Research & Development
  • Real World Evidence
  • Commercialization
  • Safety & Regulatory Compliance
  • Technologies
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.

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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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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
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SMARTSOLVE FUNDAMENTALS

Manage risk, eliminate variance, and facilitate compliance

Simplify the management of quality compliance for your small pharma business with IQVIA SmartSolve® Fundamentals.

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Solutions Safety & Regulatory Compliance Quality Compliance SmartSolve Fundamentals

CAPA MANAGEMENT

Manage CAPAs and verify effectiveness

SmartSolve Fundamentals CAPA Management helps small pharma organizations to develop a risk-based, streamlined problem resolution process. It enables you to record a problem, establish and monitor corrective and preventive actions and review the effectiveness of each CAPA. By facilitating an effective CAPA process, SmartSolve Fundamentals CAPA Management can help you shorten cycle times, resolve issues quickly and prevent recurrence helping to ensure compliance with industry, quality, and regulatory requirements.

Document Management

Securely store documents, manage revision control and route documents for review and approval

SmartSolve Fundamentals Document Management allows small pharma businesses to organize document lifecycles, accelerate reviews, and enforce document training. Users can read and sign off, prepare document profile, define training requirements and periodic reviews. The Document Management module follows a workflow with the following steps:

  • Create Document
  • Prepare Document Profile
  • Define Training Requirements
  • Approve Document
  • Finalize Document
  • Finalize Periodic Review

 

Deviation Management

Capture, verify, and investigate product and process deviation

SmartSolve® Fundamentals Deviation Management is equipped with best-practice workflows to identify, mitigate, and reduce the risks associated with unexpected events in your manufacturing process.

  • Properly document and explain product and process deviations
  • Report deviations in real time
  • Perform investigations within 30 days
  • Provides the ability to propose, initiate, and complete corrective actions
  • Release or reject implicated batches
  • Perform preventive actions

Change Management

Make informed decisions and implement changes quickly

SmartSolve Fundamentals Change Management provides you with the ability to define and assess change plans, implement individual action plan items, as well as review effectiveness for those changes that may be the result of a CAPA. It helps you to ensure consistent and compliant change control within your organization and your operations. SmartSolve Fundamentals Change Management gives your organization the tools to:

  • Manage a wide variety of changes
  • Harmonize change control procedures
  • Maintain well documented, transparent changes

DEMO

Watch the demo

Learn how this powerful workflow-driven, pre-built solution can help you to manage risk, eliminate variance and facilitate compliance.

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FACT SHEET
SmartSolve Fundamentals provides you with core quality processes to manage controlled documents, changes, deviations and CAPAs
One of the most powerful platforms designed specifically for quality and regulatory compliance.
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Allows organizations to document CAPAs, Deviations, Change Plans and manage documents as well as provide read and sign-off training

IQVIA Receives the 2023 Frost and Sullivan Enabling Technology Leadership Award

Identified as best in class North American QMS market for life sciences industry.

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Related Solutions

SmartSolve eQMS

Connected, integrated, compliant. Build, scale, and optimize your quality and regulatory workflows with SmartSolve®, IQVIA's transformative Enterprise Quality Management System, built for Life Sciences.

Quality Compliance

From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.

Regulatory Compliance

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

Contact Us