Patient Engagement Suite
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IQVIA's Integrated IRT eCOA Platform
4/25/2023
Improve study quality, accelerate decision making, and reduce site and sponsor burden by using IQVIA’s integrated Interactive Response Technology and electronic Clinical Outcome Assessment solution.
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Streamlining Clinical Trials: How To Upgrade From Paper To EDC
4/19/2023
Electronic modes have been shown to improve data quality in clinical trials. Address how equivalency can be achieved when migrating PROs from paper to ePRO.
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Fast. Flexible. Proven. IQVIA eCOA.
4/19/2023
A responsive solution, see how IQVIA's electronic clinical outcome assessments are leveraging technology to gather valuable insights about the patient and caregiver experience.
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Pharma's Frozen Assets
4/18/2023
Delve into a data-driven approach to assess the volume and value of cold chain medicines by combining IQVIA audit data with publicly available data.
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Using IRT Data To Automate And Optimize Clinical Supply
4/17/2023
Learn how clinical teams can save between $150,000 and $1 million in annual drug and shipping costs through automated supply optimization.
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Providing Drug Supply Support In Complex Environments Through IRT
4/5/2023
Learn how applying predictive data analytics can enable the creation of an ideal supply strategy capable of reducing the need for extra shipments, manual oversight, and supply waste.
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How eConsent Improves The Trial Experience For Patients And Sites
4/5/2023
In part one of this series, the author dives into how electronic consent platforms are simplifying and improving the trial experience for patients and sites.
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Biosample Tracking: A Consenting Dilemma
3/7/2023
Biosample collection is an inevitable part of most clinical trials. Learn how sponsors should be tracking every sample back to the source so as to not violate compliance issues.
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7 Considerations For eCOA Technology Solutions
3/3/2023
Choosing the right vendor, solution, and deployment model is critical for a clinical trial to be successful. As a sponsor, consider these seven best practices when selecting the best eCOA.
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eConsent For Complex Clinical Trials
10/31/2022
Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk. Learn how a feature-rich eConsent platform can simplify those processes and improve engagement.