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As a global community, IQVIA continuously invests and commits to advancing human health.
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Impacting People's Lives
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
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.
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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.
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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.
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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.
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CASE STUDY
Explore IQVIA by region
As a global community, IQVIA continuously invests and commits to advancing human health.
Americas
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Case Study
Complex Workflow and Data Collection through IQVIA Research Management Platform
Customizing Solutions with Medtech Operational and Technical Expertise
Apr 22, 2022
- Library
- Complex Workflow and Data Collection through IQVIA Research Management Platform
Leveraging the IQVIA Research Management Platform, the IQVIA MedTech team successfully created a customized data capture workflow for its sponsor. In examining the clinical use of an investigational digital slide scanner technology for pathology diagnosis, a sponsor needed to ensure its clinical research organization (CRO) partner would be capable of creating an efficient workflow and data collection system for the intricate validation protocol requirements around imaging analysis processes for two studies evaluating primary diagnoses (Study 1) and detection of pathological features (Study 2).
Download now to read the full case study on how the IQVIA MedTech team successfully met and accomplished the complex protocol requirements for both studies.