This presentation explains the role of a manufacturing plant layout design consultant in building compliant and efficient medical device manufacturing facilities. It highlights how proper facility layout planning supports regulatory requirements such as CDSCO, ISO 13485, and GMP, while improving workflow efficiency, contamination control, and audit readiness. The document covers key considerations in medical device plant layout design, common challenges faced by manufacturers, and how expert consulting helps translate regulatory expectations into practical, scalable facility designs. It also outlines a structured approach to layout planning, zoning, and execution aligned with quality and compliance requirements. Designed for medical device manufacturers, startups, plant heads, QA/RA professionals, and operations managers, this presentation provides practical insights into creating regulatory-ready manufacturing infrastructure. It reflects the manufacturing facility expertise of Operon Strategist, a consulting firm supporting turnkey medical device manufacturing projects. Learn more about manufacturing facility planning and layout design for medical devices at: https://operonstrategist.com/services/turnkey-project/manufacturing-facility/