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For information on our biotechnology and pharmaceutical capability, please contact Stephen Taylor.
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BioReliance
Upgrade of biomanufacturing facility
Glasgow, UK
![[BioReliance cleanroom modification]](graphics/biorel.jpg)
CEL was employed to undertake the upgrading of five of the eight clean rooms to grade B and containment level CL2. This involved modifications to cleanroom fabric, HVAC systems and air pressure regimes, corridor upgrades, change regimes, people flows, door and hatch interlock systems, control systems etc.
CEL responsibilities
- GMP and containment analysis
- Design and engineering of the optimum solution
- Project and construction management
- Validation support
Key features
- Work carried out with severe constraints on space and availability: production had to be maintained throughout
- High GMP and containment levels
- Extensive survey of GMP requirements and risk analysis
- Validation supervision and support
- Integrated team with subcontractors to ensure efficient use of resources and flexible delivery
Return to our biotechnology project experience.
Return to our biotechnology capability.
Return to our pharmaceutical project experience.
Return to our pharmaceutical capability.