The Aseptic Cleanroom Suite (Double Module) cGMP solution has been developed for pharmaceutical manufacturers, biotechnology organisations, CDMOs and advanced therapy providers requiring fully controlled sterile processing environments.
The facility supports aseptic manufacturing processes where environmental control, contamination prevention and validated operational performance are critical. Each suite is designed around process flow, personnel movement and material transfer requirements to support efficient, compliant production operations.
The modular configuration provides a high-performance alternative to traditional construction, enabling organisations to expand sterile manufacturing capacity, support refurbishment projects or introduce new production capability with significantly reduced programme timelines and site disruption.
These cleanroom suites are designed to meet the requirements of:
The facility is designed to accommodate critical aseptic processing equipment, including isolators, cleanroom furniture and process support systems.
Supporting areas such as preparation zones, QA spaces, storage and sterilisation facilities can be integrated within the host building to ensure efficient workflow and compliance.
Every facility is delivered with full commissioning and validation, including:
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Unit 1144 Regent Court, The Square, Gloucester Business Park, Gloucester, GL3 4AD
