New ISO Class 8 Clean Rooms for Production Facility
Lofthouse of Fleetwood Ltd engaged Integrated Life Science Group (ILS) in the design and installation management of nine new ISO class 8 clean rooms at their production facility in Fleetwood.
The expansion was necessitated by the increasing demand for Lofthouse's lozengier range.
The company recognised the need to expand production capacities to cater to this demand and concurrently extend their product portfolio.
A crucial part of the expansion plan was the creation of additional clean rooms.
ILS were responsible for the overall manufacturing facility flow design, utilities and equipment specification for the project. They also assumed full validation responsibility and qualification of equipment and utilities.
A key aim of the project with the aim of minimising disruption to the ongoing operations at the busy production site. The other aim within the design phase was to optimise the manufacturing facility flow, ensuring that the new clean rooms integrated seamlessly into the existing setup.
The specification of utilities and equipment was also another critical aspect of the project. ILS had to ensure that the selected utilities and equipment met the stringent standards required in pharmaceutical manufacturing, specifically in the production of lozenges. This involved rigorous testing and validation, providing full validation responsibility from ILS to Lofthouse of Fleetwood Ltd, ensuring that all equipment and systems were operating as intended and within specified parameters.
Despite the complexities involved, the project was successfully completed without any delays.
The nine new ISO class 8 clean rooms were seamlessly integrated into the existing setup, allowing Lofthouse of Fleetwood Ltd to ramp up their production capabilities without any disruption to their ongoing operations.
“ILS’s expertise in designing and managing the installation of our nine new ISO class 8 clean rooms was evident throughout the process. ILS ensured minimal disruption to our ongoing operations while optimising our manufacturing facility flow. Their dedication to rigorous testing and validation gave us confidence that our new facilities meet the highest standards required in pharmaceutical manufacturing.” - Lofthouse of Fleetwood Ltd.
ILS were able to deliver on their promise of minimal disruption and maximum efficiency. The new clean rooms have enabled Lofthouse of Fleetwood Ltd to meet the increasing demand for their lozengier range, while also expanding their product portfolio.
References:
- ISO14644-1:2015 - Cleanrooms and associated controlled environments - Part1: Classification of air cleanliness by particle concentration. ISO
- Whyte, W. (2001). Cleanroom technology: fundamentals of design, testing and operation. John Wiley & Sons.
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Lofthouse of Fleetwood Ltd engaged Integrated Life Science Group (ILS) in the design and installation management of nine new ISO class 8 clean rooms at their production facility in Fleetwood.
The expansion was necessitated by the increasing demand for Lofthouse’s lozengier range. The company recognised the need to expand production capacities to cater to this demand and concurrently extend their product portfolio. A crucial part of the expansion plan was the creation of additional clean rooms.
ILS were responsible for the overall manufacturing facility flow design, utilities and equipment specification for the project. They also assumed full validation responsibility and qualification of equipment and utilities.
A key aim of the project with the aim of minimising disruption to the ongoing operations at the busy production site. The other aim within the design phase was to optimise the manufacturing facility flow, ensuring that the new clean rooms integrated seamlessly into the existing setup.
The specification of utilities and equipment was also another critical aspect of the project. ILS had to ensure that the selected utilities and equipment met the stringent standards required in pharmaceutical manufacturing, specifically in the production of lozenges. This involved rigorous testing and validation, providing full validation responsibility from ILS to Lofthouse of Fleetwood Ltd, ensuring that all equipment and systems were operating as intended and within specified parameters.
Despite the complexities involved, the project was successfully completed without any delays. The nine new ISO class 8 clean rooms were seamlessly integrated into the existing setup, allowing Lofthouse of Fleetwood Ltd to ramp up their production capabilities without any disruption to their ongoing operations.
“ILS’s expertise in designing and managing the installation of our nine new ISO class 8 clean rooms was evident throughout the process. ILS ensured minimal disruption to our ongoing operations while optimising our manufacturing facility flow. Their dedication to rigorous testing and validation gave us confidence that our new facilities meet the highest standards required in pharmaceutical manufacturing.” – Lofthouse of Fleetwood Ltd.
ILS were able to deliver on their promise of minimal disruption and maximum efficiency. The new clean rooms have enabled Lofthouse of Fleetwood Ltd to meet the increasing demand for their lozengier range, while also expanding their product portfolio.
References:
- ISO14644-1:2015 – Cleanrooms and associated controlled environments – Part1: Classification of air cleanliness by particle concentration. ISO
- Whyte, W. (2001). Cleanroom technology: fundamentals of design, testing and operation. John Wiley & Sons.
