Maintaining a high level of cleanliness and sterility within a cleanroom environment is crucial for guaranteeing the quality and integrity of sensitive products or processes. Thorough validation protocols are instrumental in confirming that a cleanroom consistently meets its predefined performance standards. This involves conducting a series of tes

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

Robust design qualification (DQ) is a fundamental step in establishing the more info suitability of a cleanroom for its intended application. This thorough process involves a systematic analysis of the cleanroom's design to ensure it meets all applicable requirements and standards. DQ procedures typically include reviews of engineering drawings, si