Matrix helps medical device manufacturer reduce costly losses by eliminating air quality events
- Category: CAE
- Client: Opia
The Challenge
For medical companies to ensure their products meet quality standards, air quality is paramount. Recently, a large medical company experienced a number of air quality events associated with excursions in viable particle counts within a cleanroom. As a result, the company suffered costly lost production, downtime and cleaning expenses. They required detailed information to identify the root cause of the events and provide feedback on potential remedial solutions.
The Solution
OPIA chose Matrix to build a CFD model of the cleanroom. Matrix has the specialised experience required to conduct cleanroom simulations. Utilising the world’s most comprehensive CFD solution, STAR CCM+, Matrix can not only perform advanced analysis but presents solutions to prevent recurrence of air quality events.
OPIA performed flow tests on all the air supplies and returns, which confirmed that the model was simulating actual flow conditions in the room. The CFD model was used to calculate velocities and pressures within the room and most importantly the air residence time. This led to the identification of the location of critical dead zones within the room where non-viable particles are likely to settle. A particle tracking multiphase simulation was also performed to help OPIA engineers understand how particles of different sizes would be transported throughout the cleanroom so that accurate decisions could be made to re-design the layout and flow rates of air supplies.
The Result
The CFD model developed by Matrix was able to identify the critical region within the cleanroom. Strong agreement was observed between the location of high residence time areas and non-viable particle counts as measured by OPIA. Matrix provided practicable recommendations to improve air-flow within the cleanroom. As a result, the medical company has eliminated air quality events, preventing losses estimated in the range of hundreds of thousands of US $ per year in production under quarantine, extraordinary cleaning processes of the cleanroom and the associated impact on the regular operation of manufacturing operations.