Delivering novel CNS therapies is scientifically, medically and operationally complex. At IQVIA, we have more data and insights than ever before to drive innovation forward.
With over three decades of experience across neurology, neurodegenerative diseases, psychiatry, sleep, CNS rare diseases and pain, our CNS team can help you design and deliver complex clinical trials.
We back your passion and expertise with a team of CNS therapeutic experts, data scientists, project leaders and analysts who fearlessly strive to improve the lives of patients.
Our CNS team has a broad range of backgrounds and specialties, and we stand united with a singular focus: delivering innovative clinical trial solutions that drive new therapies to market.
As one of the highest areas of unmet need, CNS diseases are diverse, occurring at every life stage with varying severity. With fewer early-stage trials and a higher attrition rate, CNS clinical research presents a higher level of risk.
Foremost is the risk of an inconclusive trial result.
Given the high degree of complexity associated with the diagnosis and measurement of change in neuropsychiatric disorders, it is important to have a development partner with scientific expertise, operational resources and vast data assets to help you reach the right patients for the trial.
Global variability in data collection and reporting add further challenges to CNS clinical research. The need to collect and synthesize this data is pivotal to your trial’s success.
Our dedicated team of brave minds will help you manage risk and find the right path to success by harnessing the power of the IQVIA Connected Intelligence™. This holistic approach integrates our domain expertise, unparalleled data, advanced analytics and fit- for-purpose machine learning to produce innovative approaches that get your medicines to patients faster.
Connected Intelligence enables our experts to consistently deliver excellence via
Learn about the potential to advance Alzheimer's Disease trials through advanced neurodegenerative disease reference testing services and validation of innovative diagnostic biomarkers.
Access new resources for advanced therapy development, from candidate identification through market authorization.
Bring trials directly to patients to improve access and engagement, increase quality and shorten timelines.
Build on our experience of more than 245 rare disease studies in 96 countries to fulfill your promise of hope to millions around the world.
Get in touch today to discover the right solutions for you.
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