SmartSolve eQMS
SmartSolve eQMS: Simplify quality compliance management
The complete eQMS solution to simplify quality compliance management
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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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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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COMPLIANCE, SAFETY, REG PRODUCTS
IQVIA Vigilance Platform
Commercial Compliance
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Quality Compliance
SmartSolve eQMS
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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At IQVIA your potential has no limits. We thrive on bold ideas and fearless innovation. Join us in reimagining what’s possible.
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Explore IQVIA by region
As a global community, IQVIA continuously invests and commits to advancing human health.
Americas
Europe
Asia & Oceania
Middle East & Africa
EMEA Thought Leadership
IQVIA Receives the 2023 Frost and Sullivan Enabling Technology Leadership Award
Identified as best in class North American QMS market for life sciences industry.
How can you improve product performance and patient safety while reducing costs?
SmartSolve Postmarket Surveillance
Eliminate manual, repetitive tasks so you can focus on delivering safer, more effective products – faster. IQVIA’s SmartSolve Postmarket Surveillance is your complete, SaaS approach for postmarket surveillance (PMS) and provides best practices for centrally managing all post market surveillance activities. Learn More.
IQVIA SmartSolve™ Regulatory Connector
Simplify, automate and integrate your compliance response times, accuracy, predictive planning and efficiency with IQVIA SmartSolve™ Regulatory Connector.
SmartSolve is powered by IQVIA Connected Intelligence
Connected Intelligence is our innovative, interconnected approach that helps to drive operational efficiencies, increase speed, and improve accuracy and compliance performance.
A Next Generation Quality Management Solution
Every day you depend on your quality system to drive the processes that improve product quality, ensure patient safety and help maintain regulatory compliance. A mature, compliant quality system requires a harmonized, integrated approach. That’s where IQVIA SmartSolve EQMS comes in.
Learn More
Event
5th Annual European Medical Device and Diagnostic Post Market Surveillance Conference
October 4, 2023 - October 5, 2023
Fact Sheet
IQVIA™ SmartSolve® Fundamentals for Pharma
Simplify the management of quality compliance for small businesses.
White Paper
IQVIA Receives the 2023 Frost and Sullivan Enabling Technology Leadership Award
Identified as best in class North American QMS market for life sciences industry
Event
6th Annual European Medical Device And Diagnostic Quality Assurance & Control And Supplier Quality Management Conference
March 21, 2023 - March 23, 2023
Fact Sheet
SmartSolve® Automated Validation Script Authoring and Execution
Shorten the SmartSolve validation process from weeks to days
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