Article | December 18, 2025

Second Annual CRO Summit Addresses Cost, Complexity, And Collaboration In Clinical Trials

By Nancy Lamontagne, NCBiotech Writer

CRO Summit 2025 panel resized
From left, Jasmina Jankicevic, CMO, Indero; Catherine Tyner, AG Mednet; Claudia Christian, CCO, FHI Clinical Inc.; and Trish Landry, senior vice president of clinical operations, Beaufort CRO

Clinical trials are becoming increasingly complex and costly, creating pressure for sponsors and contract research organizations (CROs) to rethink traditional approaches. Industry leaders are emphasizing collaboration as a critical strategy to overcome these challenges. By fostering stronger partnerships between CROs, sponsors, and technology providers, organizations can streamline processes, reduce inefficiencies, and accelerate timelines without compromising quality.

Key discussions center on leveraging data-driven insights, adopting innovative trial designs, and integrating advanced technologies to manage rising costs and operational hurdles. The growing importance of patient-centric models and decentralized trials also highlights the need for adaptability in a rapidly evolving regulatory landscape. For stakeholders seeking to remain competitive, understanding these dynamics is essential.

Explore how collaboration and innovation are shaping the future of clinical research and what strategies can help organizations thrive in this environment. Access the full insights to learn actionable strategies for optimizing trial execution.

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