This session will explore how regulatory system strengthening and harmonization can act as a catalyst for regional pharmaceutical manufacturing in Africa, ensuring access to quality-assured medicines and building a resilient health ecosystem.
Learning Objectives
1. Discuss the role of regional regulatory harmonization initiatives in reducing duplication, and improving patient access 2. Examine how collaboration between manufacturers and regulators can streamline product development, improve compliance, and reduce time-to-market for essential medicines 3. Share lessons learned to inform future efforts and actions to support supply chain resilience
Wednesday June 17, 2026 11:40am - 12:10pm EDT Content HubThe Pennsylvania Convention Center 1101 Arch Street Philadelphia, PA 19107 USA
What if protocols weren’t documents - but executable trial blueprints? Learn how protocol digitization into structured USDM content, combined with clinical operational data, enables orchestration across systems to streamline and improve trials.
Learning Objectives
Identify how digital protocols and structured USDM models improve clinical operations and accelerate trial timelines through ecosystem orchestration. Evaluate how site operational data generates insights that streamline execution and improve protocol design. Learn how industry peers are approaching protocol digitization, including key challenges and lessons learned.
Wednesday June 17, 2026 12:20pm - 12:50pm EDT Content HubThe Pennsylvania Convention Center 1101 Arch Street Philadelphia, PA 19107 USA
