Insight Brief
Bridging Borders: IQVIA’s Expertise in Global Clinical Trial Management
Unlocking global clinical trials with IQVIA FSP Country in a Box: strategies for seamless expansion
Jan 05, 2026
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Expand Your Global Clinical Trials with Confidence

Breaking into new markets can feel complex—but it doesn’t have to. This article explores the essential strategies and practical steps for successful country expansion in global clinical trials, helping you overcome common challenges like site feasibility, regulatory intelligence, and local expertise.

Why Geographic Diversity Matters

Expanding into diverse regions isn’t just a growth strategy—it’s a competitive advantage. From recruiting representative patient populations to improving cost efficiency and accessing untapped markets, geographic diversity drives better outcomes.

That’s where IQVIA’s FSP Country in a Box comes in. This innovative solution empowers organizations to make informed decisions about target countries and seamlessly plan and execute clinical activities worldwide.

What You’ll Learn

  • How to navigate local regulations and ensure compliance with data privacy standards
  • Why addressing country-specific requirements—such as CRO licenses and CRA residency status—is critical to avoiding costly delays
  • Practical insights into logistics, supply chain management, cultural and language considerations, and financial contracting

Tailored Support for Every Step

IQVIA’s FSP Country in a Box offers flexibility and personalized support to simplify global trial expansion. From strategy to execution, we help you mitigate risks, accelerate timelines, and unlock new opportunities.

Ready to expand with confidence? Discover how IQVIA can help you take your clinical trials further, faster.

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