Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
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SEE LATEST REPORTSBy making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.
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SEARCH JOBSOngoing challenges with cost and time-to-market have created increasing pressures for sponsors to optimise their clinical trial delivery. This webinar explores some of the key headwinds for clinical trial delivery in addition to the tools, technologies and processes that are being leveraged to address these. The evolution of outsourcing strategies is discussed along with a focus on diverse Functional Service Provider (FSP) models.
These FSP delivery models will be discussed, looking at how they can be leveraged to address specific needs and requirements, their pros and cons, as well as the key deciding factors for how and when they should be employed.
Key takeaways from the webinar
Ian Pemberton
VP Clinical Operations
Stephen Evans
VP Clinical Operations
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Explore our end-to-end, full service clinical development capabilities including Therapeutics expertise, Development Planning, Phase I early clinical development, Phase IIb/III and Phase IV Trials, Regulatory Submission and Post-Launch Studies.