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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.
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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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When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
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Choose a Region
Explore IQVIA by region
As a global community, IQVIA continuously invests and commits to advancing human health.
Americas
Argentina Brazil Central America and Caribbean Colombia Mexico United States
Europe
Adriatic Netherlands Belgium Nordics Bulgaria Poland Czech Republic Portugal Germany Romania Spain Россия и СНГ France Slovakia Greece Switzerland Hungary Turkey Ireland Ukraine Israel United Kingdom Italy
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IQVIA RIM Smart Labeling

RIM Smart Labeling

Drive change with IQVIA's Pioneering, Scalable Label Information Management System, RIM Smart Labeling.

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Solutions Safety & Regulatory Compliance Regulatory Compliance IQVIA RIM Smart Labeling

IQVIA RIM Smart Labeling

Our next generation label information management solution helps to simplify your labeling activities by orchestrating multiple, disconnected processes and solutions in a single, user friendly labeling solution delivering real-time global transparency and significant efficiency gains.

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IQVIA RIM Smart Labeling

OUR LATEST THINKING ON REGULATORY COMPLIANCE

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Innovating Regulatory Services: Benefits of End-to-end Regulatory Labeling Revamp
By: Cham Williams, Jane Reed
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Real World Pharmaceutical Labeling Management: from change trigger to implementation
Blog
Technology's role in labeling and regulatory additional risk minimization measures (aRMM)
By: Cham Williams
Fact Sheet
IQVIA RIM Smart

Regulatory Information Management
Fact Sheet
IQVIA RIM Smart Submission Management
Webinar
The Future of Documents: Structured content and integrated data
February 2, 2022
Blog
Data is the focus for regulatory submissions
By: Cham Williams
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