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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.
REAL WORLD EVIDENCE OVERVIEW
Real World & Health Data Sets
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Medical Affairs
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Health Data Apps & AI
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Health Data Transformation
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Study Design
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Evidence Networks
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Health Economics & Value
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Regulatory and Safety
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Natural Language Processing
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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
COVID-19 & Commercialization
COVID-19 & Commercialization (desc)
Launch Strategy & Management
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Pricing & Market Access
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Healthcare Professional Engagement
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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.
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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Enterprise Information Management
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Performance Management & Insights
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Provider Reference Data Network
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Customer Engagement
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Safety, Regulatory, Quality Compliance
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The IQVIA difference
CLINICAL PRODUCTS
Planning Suite
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Trial Management Suite
Clinical Data Analytics Suite
COMMERCIAL PRODUCTS
Information Management
Launch Strategy & Management
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COMPLIANCE, SAFETY, REG PRODUCTS
Commercial Compliance
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REAL WORLD PRODUCTS
Data Profiling
Patient Profiling
HCP Profiling
Market Profiling
Health Data Transformation
Natural Language Processing
CASE STUDY
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
White Paper
Conducting Effective Post-Market Safety Studies for Medical Devices
Feb 17, 2022
- Library
- Conducting Effective Post-Market Safety Studies for Medical Devices
The medical device regulatory landscape is evolving and there is an increased demand to generate high-quality safety data in a practical, cost-effective and efficient way. This white paper provides information on the different types of post-market safety studies, the importance of applying a patient-centric approach, and how to maximize data quality and integrity.