ABOUT IQVIA TECHNOLOGIES
IQVIA Technologies develops purpose-built solutions on a future-state architecture to enable connected intelligence across the entire life sciences product lifecycle. Under our Orchestrated Clinical Trials (OCT) platform, we’re driving smarter, faster trials for sponsors, sites and patients, with more than 20 market-leading, cloud-based products and tech-enabled services. These best-of-breed technologies are grouped as Digital Suites and are available independently of our CRO services, with support models customized to meet your specific business needs.
DIGITAL SITE SUITE
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![GettyImages-944060504 coworkers computer]( "One Home For Sites Partnership Program Guide")
When sponsors of trials adopt IQVIA One Home for Sites, they reduce the burden on their clinical research sites and on their own organizations.
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![GettyImages-1168921630 drug study]( "Study Start-Up Challenges: Hard Realities, Effective Strategies")
Launching a study is complex, and the time between protocol approval and the first patient visit has increased dramatically. How can companies reverse this trend and accelerate study start-ups?
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![GettyImages-1314931058 doctor computer]( "Introducing One Home for Sites")
Join the movement to increase clinical research site capacity. IQVIA One Home for Sites serves as a neutral aggregator, connector, and communicator of the key systems and tasks sites need to perform.
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![Digital technology-GettyImages-826921436]( "Accelerating Site Activation: Examples From Novartis And IQVIA")
As protocols and studies become more complex, using technology to offer sites in-depth expertise and guidance is more important than ever to launch studies on time.
PATIENT ENGAGEMENT SUITE
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![GettyImages-486359855 business ipad hospital]( "eCOA Licensing Guide")
In this comprehensive guide, IQVIA's eCOA library and licensing specialists, Kayla Doyle and Piero Bindi, explore five essential steps for obtaining licenses for the assessments required in your clinical trial.
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![GettyImages-1444062860 nurse patient clinical]( "Medical Device Trial Integration")
Each device, with its unique technology and study parameters, presents a distinctive challenge that demands precision at every turn. Learn how we can help to revolutionize your medical device trial journey.
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![right size econsent web thumb]( "Right-Size Your eConsent Approach")
Delve into the art of tailoring the eConsent experience to match the specific needs of your study and patients, such as how to craft patient-centric eConsent documents, select appropriate delivery models, and more.
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![IQVIA Innovations in IRT web thumb]( "Innovations In IRT")
Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.
CONTACT INFORMATION
IQVIA Technologies
4820 Emperor Blvd
Durham, NC 27703
UNITED STATES
Phone: 1-888-336-3748
Contact: Turquiose Ross, MBA
DIGITAL PLANNING SUITE
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![GettyImages-1353835415 q&a]( "IQVIA GrantPlan Questions And Answers")
IQVIA GrantPlan experts recently discussed how to use benchmark data to create fair market value budgets, given sky-rocketing inflation and attrition rates.
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![GettyImages-1441381006 budget talks]( "5 Tips For Negotiating Clinical Trial Budgets In Inflationary Times")
Rapid inflation and staffing shortages make it more difficult for sites and sponsors to agree to a budget. Explore five ways teams can respond during these inflationary times.
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![GettyImages-1457639530 inflation report]( "The Impact Of High Inflation And The Great Resignation On Clinical Site Budgeting")
The twin pressures of inflation and attrition prolong negotiations between sponsors and clinical sites, stalling drug development. Sponsors need up-to-date, reliable benchmark data to negotiate fair market value budgets.
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![GettyImages-179973335 budget]( "IQVIA GrantPlan: Confidently Forecast And Budget Investigator Grants")
Learn how to build more accurate study budgets while reducing costs and improving start-up times.
