Increasing Productivity in Clinical Research - Life Sciences Today Podcast Episode 48
Why It Matters
By dramatically shortening trial start‑up and operational delays, Yandu’s solution can reduce drug development costs and bring life‑saving therapies to patients faster.
Key Takeaways
- •Clinical trial timelines waste 12‑18 months in “white space”.
- •Yandu’s site‑centric platform cuts feasibility time by 50%.
- •Automated, personalized follow‑ups reduce task completion from three weeks to five days.
- •Reusable site data accelerates future trials and improves sponsor‑site relationships.
- •Faster trial start‑up saves teams ~39 workdays annually per project.
Summary
Life Sciences Today host Danny Lieberman interviews Zena Sarif, founder of Yandu, about the chronic inefficiencies that prolong clinical‑trial timelines and how her startup aims to streamline the process.
Sarif explains that up to 12‑18 months of a drug’s development are spent in a “white space” between trial phases, where sites are slow to respond and data are siloed. Yandu’s platform replaces project‑centric data stores with a site‑centric architecture, offering login‑free, automatically structured communication and AI‑driven, personalized follow‑ups that cut feasibility timelines by half and reduce task completion from three weeks to five days.
The company reports that 91% of sites finish tasks within five days, shaving 13 weeks off site‑selection and saving teams roughly 39 workdays per year, while creating reusable knowledge that accelerates future studies.
If adopted broadly, these efficiencies could compress drug‑to‑market cycles, lower R&D costs, and improve patient access to therapies, signaling a potential shift in how sponsors and CROs manage clinical operations.
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