Outsourced Biomanufacturing

© Hedley Rees

Discover how strategic alliances, flexible facility design, and advanced outsourcing models—including CROs, 3PLs, and CDMOs—are reshaping efficiency, scalability, and resilience in biopharmaceutical development and production.

What You Will Learn

• Strategies for building successful outsourcing partnerships with CROs, 3PLs, and CDMOs
• How modular and single-use facilities enable rapid scale-up and multi-product readiness
• Methods for mastering regulatory trends, cost control, and sustainable supply chain management

Who Should Join

• Biopharma professionals and CDMO operations leaders
• Pharmaceutical supply chain managers and strategic partnership officers
• R&D specialists, regulatory affairs experts, and QA/QC professionals
• Business development executives and automation technologists
• Solution providers supporting outsourced biomanufacturing and supply chain innovation

Speaker: Hedley Rees, Founder and Managing Consultant at PharmaFlow

He is a twice‑published author with Wiley (NJ), namely “Transforming the Pharmaceutical Supply Chain” 2025 and “Supply Chain Management in the Drug Industry: Delivering Patient Value for Pharmaceuticals and Biologics,” 2011.