11.12.25 -- Working With Leaders Who Have 'Rounded Corners'

Learn how predictive modeling, powered by real-world data, is essential for proactively solving patient enrollment challenges and optimizing site performance to accelerate your clinical trials.

Drugs have become more lipophilic and complex in structure over time. Innovative strategies are needed to improve the bioavailability of these new drugs.

Learn how sponsors and CROs are using agentic AI to eliminate the unproductive time caused by manual, sequential processes and fragmented data systems.

Find embedded regulatory expertise that strengthens compliance, accelerates timelines, and ensures audit readiness—without adding headcount. Get strategic, on-site support tailored to your regulatory landscape.

For biopharmas looking to outsource their early phase development, consider working with a CDMO partner that has the knowledge and experience to navigate microbial fermentation and complex process development.

Explore key challenges in accessing and preparing analytics-ready clinical data, how FAIR guiding principles can help maximize the value of clinical trial data, and the impact of innovative analytics.

In this presentation, we share insights into how a culture-forward FSP framework enhances operational efficiency, strengthens partnerships, and helps organizations adapt to growingly complex research.

Early biostatistical input strengthens trial design, reduces risk, and ensures meaningful outcomes while strategic involvement drives smarter decisions. Learn why timing and collaboration matter.