Delivering validated, highly regulated manufacturing environments within a live operational facility.
Terumo Aortic required a significant upgrade to its UK headquarters and manufacturing facility to support growth in the surgical grafts market. The challenge lay in delivering complex, GMP-compliant cleanrooms and sterilisation facilities within an operational site, while meeting strict regulatory, quality, and safety requirements.
The programme needed to balance technical excellence, programme certainty, and quality assurance, ensuring that new facilities could be licensed, commissioned, and validated without disruption to ongoing manufacturing operations.
