The right pediatric program to deliver your medicine sooner.

Providing new treatments for children requires careful planning and expertise – with patient safety at the center of everything you do.
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Let expertise be your guide

Successfully navigating the road to developing and delivering pediatric products requires a specialized mix of scientific, therapeutic, regulatory and operational expertise to ensure your pediatric studies are successfully planned and executed.

From the earliest planning stages of clinical development, through launch and real-world assessment, pediatric expertise is key to ensuring you are asking the right questions to meet the specific needs of infants, children and adolescents.

IQVIA's Experience

364 pediatric studies

conducted across 101 countries between 2013 and 2018

From start to finish, we are here

At IQVIA, we are prepared to provide tailored, informed support throughout your journey. We can help

  • Develop your product’s Pediatric Investigation Plan (PIP) and/or Pediatric Study Plan (PSP)
  • Recommend alternative study designs through the use of modeling, simulation and real world data
  • Navigate complex and unique regulatory requirements for pediatric clinical research
  • Connect you to a network of specialized pediatric study sites
  • Identify, consent/assent and retain pediatric patients and their families throughout your program

Pediatric Center of Excellence

Experts from across IQVIA come together to help you conceptualize and execute your pediatric studies. The group is charged with advising on the conduct of pediatric programs to ensure the right strategy and the right level of oversight, counsel, training and collaboration is applied to your project. Identify the right path to fulfill pediatric safety requirements and deliver a product that meets the unique needs of infants, children and adolescents, from trial environments into their everyday lives.

Solutions you may be interested in
Protocol Design

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

Real World Data and Insights

Learn more about the federated evidence networks and massive, non-identified global databases that inform our real world solutions.

Virtual Trials

Bring trials directly to patients to decrease costs, increase quality and improve access.

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