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Feasibility as a Service

Product Information
Patient Engagement & Recruitment
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Expert-led, data-driven feasibility to de-risk trial design and execution

Trial design and site selection decisions are too costly to get wrong.

Sponsors today face escalating challenges:

  • 60% increase in protocol amendments since 20151

  • 7 months longer for trial timelines, 2020-242

  • $40K daily costs for Phase II and III trials3

  • $500K in lost sales daily3 from delays

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Our Solution: Feasibility as a Service (FaaS)

FaaS is an expert-led, data-driven assessment that helps determine protocol viability, site selection strategies, recruitment plans, and mid-trial rescue decisions. Powered by Citeline's gold-standard Sitetrove and Trialtrove tools, our next-generation feasibility is now delivered as a service anchored in an independent and objective perspective to guide confident decisions.

With dynamic, decision-ready outputs, we help sponsors and their development partners de-risk design, adapt in real time, and keep studies on track without adding operational burden.

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References

1 New Benchmarks on Protocol Amendment Practices, Trends and their Impact on Clinical Trial Performance

2 https://www.statista.com/statistics/1419920/biopharma-clinical-trial-cycle-time/

3 New Estimates on the Cost of a Delay Day in Drug Development