As the pharmaceutical industry faces increasing pressures for efficiency, safety, and regulatory compliance, engineering excellence plays a critical role in ensuring smooth daily operations. This session will explore best practices in engineering design, focusing on Greenfield (new) projects, where the foundational decisions made during the design phase significantly impact the future performance, cost, and regulatory compliance of pharmaceutical manufacturing operations. Attendees will gain valuable insights into the key aspects of design that drive operational excellence, sustainability, and regulatory adherence. In this session, you will learn how to:
- Navigate challenges in the design of Greenfield projects, ensuring compliance with industry standards and regulatory requirements.
- Align design with operational goals to enhance efficiency, reduce downtime, and minimize operational costs.
- Foster continuous improvement in the design phase to build scalable and adaptable manufacturing environments.
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