This webinar summary argues that MedTech and pharma companies need unified electronic quality management systems to meet rising regulatory and data‑handling demands. Successful deployment hinges on controlling scope, dedicating resources, harmonizing processes and understanding organizational culture. Companies must consider scale, therapeutic area and route to market when choosing an eQMS and evaluate integration with ERP or legacy systems. Drivers for integration include exploding data volumes, widespread digital devices and stricter regulatory requirements. A unified eQMS streamlines safety, quality and compliance processes, but success requires rigorous planning, communication and management buy‑in.

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