Case Study: ProPharma
Cytotoxic Facility and Sterile Facility
ProPharma is a pharmaceutical company specialising in drug formulation development and small scale sterile manufacture of liquid fill or freeze dried parenteral's for phase I and II clinical trials to MHRA and FDA cGMP standards.
For this project, Bassaire were awarded the contract to provide a complete turnkey project for the production facility, which consisted of two modular suites, one non-cytotoxic suites and one cytotoxic suites, which are physically separate and independently serviced.
The services provided by Bassaire were for the design, planning and building control, construction/installation, testing/commissioning and complete validation, from inception to completion.
The suite consists of grade A, B, C and D areas, which were all fully validated to MHRA standards.
ProPharma case study datasheet (PDF) 304 KB
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