Accelerate clinical development with the IQVIA CORE

Work faster, leaner and smarter from study design to submission, with customized research solutions powered by the IQVIA CORE. Put our data, analytics, networks, and expert knowledge behind your next trial.
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As science moves faster, research keeps pace

From emerging biotech firms to the largest global pharmaceutical companies, IQVIA's CORE-powered Clinical Development approach helps you match the pace of innovation with integrated solutions, and gives you the flexibility to match capabilities precisely with research needs.

We’re committed to providing solutions that help you innovate with confidence, maximize opportunities, and ultimately drive patient outcomes forward. The IQVIA CORE can connect you to innovative trial solutions like precision site selection, centralized monitoring, automated safety case processing and global regulatory expertise.

IQVIA Outcomes

25% lower

study costs using IQVIA's risk based monitoring
Internal analysis, IQVIA Risk Based Monitoring Analytics, June 2019
IQVIA's Expertise

4,600+ data scientists

Including statisticians and analytic developers

R&D capabilities powered by the IQVIA CORE

  • A global network of trial sites to optimize patient recruiting and research focus
  • Advanced analytics leveraging machine learning and artificial intelligence
  • Real world data to support enriched trials and innovative study design
  • Regulatory knowledge across more than 100 global markets
  • Digital enablement including virtual trials and synthetic study arms

IQVIA Risk-Based Monitoring approach

Analytics drive new efficiencies

Project management

IQVIA project managers connect you to the full power of IQVIA’s data, technology and trial expertise to bring your study in on time and on budget. With the power of the CORE, we can identify challenges and resolve those earlier, keeping you informed at every step along the way.
IQVIA's Expertise

4,600+ data scientists

Including statisticians and analytic developers
related solutions
Protocol Design

Assess your protocol against real world evidence using advanced analytics, and reduce the risk of costly amendments.

Phase I Trials

Leverage a global network of Phase I clinical pharmacology units to build diversity in patient populations and access a range of geographic regions for early clinical development (ECD) programs.

Site Identification

Identify the best performing sites for your trial in less time with new machine learning and predictive modeling methods.

Patient Recruitment

Predict enrollment more accurately and increase the number of patients per site using data-driven patient recruitment solutions.

Global Laboratories

Access central labs around the globe through Q² Solutions, a joint venture between IQVIA and Quest Diagnostics.

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