Upgrade of a solid dose facility (Tablets, liquids and creams). This project was classified to an ISO 7 Standard.
Located within an existing building in Chaiwan, Hong Kong Island, we worked closely with the client to upgrade this existing pharmaceutical manufacturing facility to meet the GMP requirements of the Hong Kong Government.
Working with the client to establish process flows and the logistics of equipment installation, we developed the design layout and executed the project in phases to ensure production was maintained at all times.
- Modular Cleanroom Walls and doors
- Cleanroom Ceilings