Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
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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
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
Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
COMMERCIALIZATION OVERVIEW
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
COMPLIANCE OVERVIEW
When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
TECHNOLOGIES OVERVIEWExplore our library of insights, thought leadership, and the latest topics & trends in healthcare.
DISCOVER INSIGHTSAn in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
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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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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 new expert analyst is here. Be at the forefront of data-driven decision-making with a new generative AI tool that enables you to interact with our products and solutions like never before. Get results you can trust, faster.
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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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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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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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Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm.
LEARN MOREOur mission is to accelerate innovation for a healthier world. Together, we can solve customer challenges and improve patient lives.
LEARN MORECareers, culture and everything in between. Find out what’s going on right here, right now.
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"Improving human health requires brave thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.
SEARCH JOBSBe a part of the only platform that’s bringing the industry together to help sites survive and thrive, along with their patients. Your participation in the One Home for Sites Partnership Program will build the clinical trial ecosystem and transform the site experience – to benefit all.
With sites now averaging more than 50 application logins to manage across their trials, they’re pushing back on sponsors and saying “no” to trials that are too complex. Some sites are even charging sponsors for every portal they’re asked to use.
The result: Technology vendors of all sizes and specialties are being seen as the source of clinical trial inefficiencies, rather than the solution. Even large software providers with unified platforms bring limited relief. Tech adoption will slow for everyone if something doesn’t change.
One Home for Sites enables technology partners to come together in a neutral platform, while each delivers its distinct functionality and benefits to sites, sponsors, and CROs. Your software shines, because One Home’s main role of aggregation and communication across systems and studies is working behind the scenes, providing:
Access this IDC Research Note covering IQVIA One Home for Sites and its potential to address the multisystem-access fatigue that sites are experiencing.
Explore IDC’s point of view that the One Home product launch underscores IQVIA's leadership in unifying the industry to transform clinical trials.
Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. With over 20 years of groundbreaking technological innovation across more than 30,000 trials and 9 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and the largest patient-level historical clinical trial data set in the world. More than 1 million registered users across 2,100+ customers trust Medidata’s seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes company (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com and follow us @Medidata.
Welcome to the Greenphire Patient Convenience platform! Using this all-in-one solution, you have the tools you need to remove financial, logistical and administrative burdens for both the participant and site staff. . Greenphire’s ClinCard reimbursement software has earned an impressive 91% site satisfaction rate from global sites, while our robust ConneX Travel Services delivers robust travel support for patients - getting them local and long-distance transportation and lodging. Our solutions deliver peace of mind for patients, and eliminate site administration, reducing processes which used to take 30 minutes or more down to seconds. Learn more about Greenphire here: https://greenphire.com/
Clario delivers a comprehensive platform helping sites and patients navigate their clinical trial journey: enabling site personnel to schedule and manage patient assessments throughout the visit schedule; providing a comprehensive view of patient activity and trial progress, and a single access point for Clario applications.
Signant SmartSignals® Unified Platform, from Signant Health, offers sponsors and sites a truly integrated, contiguous platform and experience across the key technologies in the clinical trial tech stack, including EDC, RTSM, eCOA, eConsent, telehealth, and more. One sign on. One database. Purpose-built to eliminate tech fatigue at sites and enhance the patient experience.
TruLab is a leading provider of technology for clinical trial oversight, dedicated to enhancing data quality and mitigating risks in drug development. TruLab supports top pharmaceutical companies and biotechnology companies to speed patient screening and enrollment, ensure data integrity, and prevent protocol deviations.
Viedoc designs engaging software for the life science industry. By accelerating clinical trials on all levels, its solutions support major pharmaceutical, biotech, and medical device companies, as well as renowned research institutions worldwide. Headquartered in Uppsala, Sweden, Viedoc also has offices in America, France, Japan, Vietnam, and China. Since our inception in 2003, over 1 million patients in more than 75 countries have participated in studies powered by Viedoc.
Zelta by Merative is a clinical trials solution business that includes a clinical data management and acquisition platform, as well as consulting, enablement, and extension services. Zelta’s unified cloud-hosted platform has supported over 4,100 trials to date across all phases and complexities of research, including more than 500 phase III trials.
Patiro was born out of a need to address the delays in clinical trials caused by patient recruitment challenges. It provides digital tools and AI to ensure timely and precise patient matching across various therapeutic areas.
One Home for Sites is an ambitious undertaking, because no single vendor or sponsor can solve an industry-wide challenge alone.
Whether you’re a tech start-up or already an industry leader, joining the One Home for Sites Partner Program makes an important contribution to the future of clinical trials
Licenses will grow as site capacity expands and the industry can run more trials. Plus, sponsors, sites, and CROs will prefer clinical technology that’s already integrated into One Home.
Equipped with seamless navigation between tasks and applications, sites will spend less time logging in and more time gaining value from your software. And you’ll see reduced development costs compared to having to deploy custom integrations.
Get access to technical documentation, One Home for Sites support, and a Community Forum to share ideas and best practices.
Please join us to help promote the value of One Home for Sites to Sponsors, Sites and vendors to increase clinical trial capacity across the life sciences industry.
Explore this guide to learn more about the benefits of becoming a One Home for Sites partner.
One Home for Sites is the only product that serves as a neutral aggregator, connector, and communicator of the key systems and tasks a site needs to perform across all the clinical trials it is conducting.
When sponsors, CROs, and tech vendors tap into the power of One Home, they amplify the benefits to sites and their own organizations.
Communicate key systems and workflow activities across multiple trials, connecting sponsors, CROs, and tech vendors.
Communication, collaboration and transparency between sites and sponsors mean trials start up and close out faster.
Increase transparency, improve communications and reduce administrative burden for all clinical trial stakeholders.
Ease the burden on your sites and make it easier and more appealing for patients to enroll and remain engaged.
