Qualification measurements for cleanrooms are a decisive factor in quality management in sectors such as the pharmaceutical, medical and semiconductor industries. They ensure that cleanrooms fulfil the required specifications and consistently meet the prescribed conditions.
In this presentation, we will talk about the phases in which we should check the cleanroom and how we can avoid problems that can affect the processes and the final product.
These measurements ensure that the controlled environment fulfils all standards requirements and that product quality is not compromised.