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From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
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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.
REAL WORLD EVIDENCE OVERVIEW
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Real World Evidence Library
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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.
COMMERCIALIZATION OVERVIEW
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.
COMPLIANCE OVERVIEW
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.
TECHNOLOGIES OVERVIEW
Orchestrated Clinical Trials
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Commercial Compliance
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Safety, Regulatory, Quality Compliance
Safety, Regulatory, Quality Compliance (desc)
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The IQVIA difference
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IQVIA Vigilance Platform
Commercial Compliance
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Quality Compliance
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Safety & Pharmacovigilance
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Explore our library of insights, thought leadership, and the latest topics & trends in healthcare.
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An in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
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As a global community, IQVIA continuously invests and commits to advancing human health.
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Fact Sheet
SmartSolve® Automated Validation Script Authoring and Execution
Shorten the SmartSolve validation process from weeks to days
Feb 07, 2023
- Library
- SmartSolve® Automated Validation Script Authoring and Execution
Get instant access
For companies who want to automate the collection of validation objective evidence while expanding coverage to reduce risk without extra people, time, or money, IQVIA introduces SmartSolve® Automated Validation Script Authoring and Execution. This patented, innovative capability enables you to streamline and manage the validation process instead of authoring or executing elaborated scripts, adapting to change more efficiently and with increased accuracy while reducing risk.
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Safety & Regulatory Compliance
Meet the challenge of changing stakeholder demands and increasing cost constraints with IQVIA's integrated technology services and analytics-driven offerings.