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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
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
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CLINICAL PRODUCTS
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REAL WORLD PRODUCTS

CASE STUDY

"Data in a Day

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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

"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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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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RESEARCH & DEVELOPMENT

Streamline drug development with innovative Biostatistics

IQVIA Biostatistics can be a competitive advantage when drug development timelines are tight. With our end-to-end data flow and proprietary technologies, and a global presence, we can get you there faster.

Our connected devices streamline data collection while our innovative and complex trial designs   allow for more efficient decision points.

Whether delivered via full-service, functional service provider or staffing, IQVIA is ready to help meet your biostatistics goals.

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Solutions Research & Development Clinical Trials Phase IIb/III Trials Biostatistics
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End-to-end biostatistical support across trials and phases

Do you need a global footprint to reach your trials goals? Or perhaps require experts to orchestrate your regulatory submission? Need specialty expertise to design and analyze your trials? Then our +1,500  biostatistical experts are ready to provide the knowledge and tools to overcome any challenge across any stage of your drug development process.

Our biostats experts provide innovation trial solutions including:

  • Adaptive designs
  • Master protocols (basket, umbrella trials) and bridging studies
  • Combination of real-world data with clinical trial data
  • External comparators
  • Precision dosing

In order to shorten timelines and extract the most value from your data, the right process is imperative. Our biostatistics experts leverage a data-collection framework to support decision making. Let us help you gain the most value from your data.

Karen Zieker
 Vice President Biostatistics
IQVIA Data Science Safety Medical

Guide your drug development with our biostatistics expertise and technology

IQVIA supports your trial holistically by applying statistical programming, patient data visualization, and pharmacokinetic expertise supported by proprietary technology.  Along with traditional biostatistics deliverables, we also leverage our knowledge in innovation designs, analysis, machine learning (ML) and technologies to guide you in development.

Innovation in healthcare

Innovation starts with developing proprietary processes, strategies, and software. To ensure you have the best start possible, we use these internally and make them available to you. These biostatistical innovations are powered by our Connected Intelligence ecosystem, combining data, expertise, and advanced analytics to provide you with unique solutions that increase productivity, reduce timelines, and allow for better decision processes. We offer the best fit-for-purpose tech-enabled solution to our customers whereas:

  • Working on our systems and getting full advantage of our data ecosystem with ready-to-use automation tools and connected CDR
  • Bringing innovation in our customers’ systems, with our implementation experts and system agnostic approach that can adapt to any environment with its interoperability
IQVIA’s Worldwide Expertise

>1500 biostatisticians

> 1,500 Biostatisticians professionals globally

IQVIA’s Expertise

>3,500 studies

>3,5000 studies executed globally

IQVIA’s Expertise

25 Registrations

25 Registrations submissions in the last 5 years.

IQVIA’s Expertise

> 10 years experience

> 10 years experience with platform studies

Strategic guidance

Clinical Development Strategies

Overview

As your biostatistics strategic partner, we help you to define a clear pathway to submission, by developing solutions which optimize your timelines, plan trials, estimate time and cost to submission. We study the effects of different options on your development strategy through technology, supported solutions, expertise, and knowledge.

Synopsis Development

With over 30 years of experience designing trials and interacting with regulatory authorities, we support sample size calculations, endpoint capture and analysis, and provide you with the optimal trial design.

Protocol Development

Whether you need biostatistical support to work through market authorizations or the experience and knowledge to effectively navigate regulatory interactions, trust our biostatistics experts to turn your synopsis into a full protocol or provide actionable changes to existing ones and provide support for regulatory interactions.

Trial Execution & Analysis

Whether a review of the database build, authoring the SAP, collaboration with statistical programmers on SDTM and ADaM creation, draft and final deliverables, interpretation of results or clinical study report support, we offer a full scope of biostatistical services and maintain full compliance with all regulatory requirements with strong QA processes.

Regulatory Submissions

Submission time is often hectic. Our experienced team will partner with you to navigate the challenges and support submission activities to the FDA, EMA and PMDA including ISS and ISE.

Our range of submission support services is wide ranging, from CRTs in eCTD format, to Define.xml.  At the same time our team can be your partner from anything as a reviewer guides to provide attendance at regulatory meetings

The right working models for you

Traditional approaches allow you to work with us on each trial independently. We provide you with the flexibility to meet changing needs.

Our Functional service provider (FSP) models provide a dedicated team to support multiple studies and enhance efficiencies as we work within your protocols and standards.

IQVIA seamlessly integrates into your statistical team; this enables you to flexibly expand your team while maintaining control.

Find out more on how we craft a custom-made solution to fit your needs.

IQVIA Commercial Technologies

White Paper
IQVIA Trial Designer
White Paper
Registries for Rare Diseases
White Paper
Consumer Health Digestives Category QuickView
Publication
Get Ahead of Consumer Health Trends Across the Globe
White Paper
Dose-Finding in Early Clinical Trials with IQVIA Trial Designer
Event
PharmaSUG 2023 - San Francisco
May 14, 2023 - May 17, 2023
White Paper
Clinical Data Flow The Foundation of a Biostatistics Ecosystem Within a Data Universe
White Paper
Recruiting Rare Disease Patients Just Got Easier
White Paper
Driving Decision Making Using Adaptive Trials
Blog
One protocol - multiple studies
Event
Applied Adaptive Design Using Subgroup Identification & Machine Learning
October 25, 2022
Blog
Are AI/ML methodologies changing how subgroup analysis is being performed for clinical trials & real-world data?
By: Kal Chaudhuri
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Data Management

Ensure you have access to insights early with connected devices and clean, analysis-ready data

Functional Services

Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.

Connected Devices

Clinical trials face increasing pressure to deliver new treatments to market faster. IQVIA Connected Devices accelerates trial outcomes with medical device recommendations that fit your clinical study, deliver cleaner data, and speed data collection and analysis with lower patient and site burdens.

Clinical Monitoring

Enhance patient safety and study quality by using data, analytics, and technology to monitor patient, site, and study performance with risk-based and centralized monitoring.

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