This case study explores the systemic challenges of establishing a robust maintenance and calibration program during the capital phase of GMP-regulated pharmaceutical facilities. Often driven by accelerated timelines and shifting priorities, the induction of assets during capital projects can lead to fragmented systems, incomplete data structures, and long-term inefficiencies. Drawing on recent project examples, this session examines the disconnect between project execution teams and operational stakeholders, and presents strategies to align technical requirements, quality expectations, and asset readiness within the constraints of project delivery. In this session, you will learn more about how to:

• Bridge the gap between capital project objectives and the long-term needs of end users in GMP-compliant environments
• Define operational success factors for asset induction beyond go-live metrics, including data completeness and calibration readiness
• Address knowledge gaps between engineering, quality, and maintenance teams through early-phase planning and collaborative frameworks