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-1464245432 payments]( "The Impact Of Clinical Trial Payments On Site-Sponsor Relationships")
The sponsor-site relationship relies on good faith, but late payments sow mistrust. Experts from BMS and CenExel Clinical Research explain how consolidating payment systems benefits both parties.
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![GettyImages-1377762347 validation]( "Crowdsource UAT: An Opportunity For Future Validation")
IQVIA, a leading health information technology and clinical research company, has introduced a new validation model for eTMF patterned after approaches used within the larger tech space.
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![ERI Quiz Looking At Computer Desk]( "Reduce Workloads And Improve Insights With Crowdsource UAT")
Crowdsource UAT, a validation model that enables testing via real, external users, can offer many potential advantages for an evolving clinical trial industry.
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![GettyImages-1408596915 eTMF]( "Achieving Faster, Simpler Validation Through Crowdsource UAT")
An approach most often seen in the larger tech space, crowdsource UAT can offer several potential advantages for the clinical trial industry and eTMF validation.
PATIENT ENGAGEMENT SUITE
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![Patient with ipad]( "How eConsent Delivers Value For Sponsors")
Delve into the data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials.
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![GettyImages-1344606074 data insights]( "Data-Driven Adaptive Trials Enhance Safety, Progress, & Economics")
By offering guidance on optimizing ROI from extensive data collections and various endpoints in clinical studies, learn how IRT technology can enhance the data-driven approach for sponsors.
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![ipad patient telehealth iStock-1038364106]( "IQVIA Integrated Complete Consent IRT eCOA")
Learn how to improve data quality and usability while optimizing trial conduct with this interoperable technology.
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![Drug development iStock-1067499066]( "Drug Accountability And Returns Management")
See how sponsors are using electronic solutions for Drug Accountability (DA) and experiencing significant increases in efficiency and accuracy that these methods provide.
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.
DIGITAL TRIAL MANAGEMENT SUITE
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![Risk-Benefit-reward-GettyImages-1264804060]( "Risk-Based Quality Management")
Effectively plan and monitor clinical trials with IQVIA Technologies' configurable, SaaS-based solution that helps you mitigate risk and identify the "next best action."
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![Risk GettyImages-1165478951]( "What Is All The Uproar About Risk?")
Do you ever feel like your trial could be at risk? What if you don’t catch missed adverse events or something more important? Find out the ways you can combat risk in your clinical trial.
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![GettyImages-1322205575 data ps]( "Integrated Clinical Monitoring – Technology Enabling Data To Talk!")
When you think about Integrated Monitoring, what does that really mean? Learn how technology and monitoring fit together intelligently to reduce your workload within clinical trials. Find out more in the third blog within this RBQM series.
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![Medical data risk iStock-1185375169]( "All I Want From My RBQM Solution")
Today’s technology is capable of automating risks initially and continually throughout a trial. Find out more about these solutions in the second blog within this RBQM series.
