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Protocol amendments have long been a challenge for the drug development industry given their impact on clinical trial costs and timelines. More than half of finalized protocols undergo an amendment and about half of these are avoidable. Investing in protocol optimization solutions to improve the design process has proven to be essential.
In this webinar, solutions for protocol optimization are shared along with examples demonstrating how IQVIA's data-informed protocol assessment makes an impact on protocol design by reducing risks that could lead to amendments.
Three key take-aways
Tammie Nguyen
Design Analytics Director