Cytotoxic facility and sterile facility

Cleanroom case study: ProPharma

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.