Bring your biosimilar to market faster.

The race is on to bring your biosimilar to market faster. Boost your progress by asking the right questions and creating a customized approach to meet your goals.
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Expert-led decision support

It is challenging to navigate biosimilars regulation and the payer landscape, provide real world evidence to physicians, and compete for the right sites and patients. IQVIA an help you overcome these obstacles and make better decisions throughout your study's lifecycle using a customized approach backed by expertise in more than 13 therapeutic areas.

It starts when you leverage the power of the IQVIA CORE. This is how we use unparalleled data, transformative technology, advanced analytics, and scientific expertise to help achieve study goals and bring biosimilar drugs to market faster.

Powered by the IQVIA CORE

  • Experts that have built trial designs for more than a dozen compounds over the past decade, reaching 20 unique biological targets
  • Transformative technology that allows real-time access to operation-critical information to accelerate study timelines
  • Unparalleled data sources available to optimize biosimilar drug development
  • Advanced analytics capabilities to identify the right sites – inclusive of established site relationships – allowing for faster start-up and accelerated patient enrollment
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