Maintaining a high level of cleanliness and sterility within a cleanroom environment is essential for securing the quality and integrity of sensitive products or processes. Stringent validation protocols are critical in demonstrating that a cleanroom consistently meets its predefined performance standards. This involves executing a series of tests

Renrumscertificering spiller en central/afgørende/nødvendig rolle i at sikre, at virksomheder indenfor renrumsmiljøet opfylder de gældende brancheoverensstemmelseskrav. En certificering more info garanterer, at processer og procedurer er tjekket/dokumenterede/valideret for at minimere kontamination og garantere højeste kvalitet på produkter/a

Robust design qualification (DQ) is a critical step in establishing the suitability of a cleanroom for its intended purpose. This rigorous process involves a systematic assessment of the cleanroom's configuration to ensure it meets all necessary requirements and standards. DQ activities typically include reviews of engineering drawings, simulations