Maintaining a high level of cleanliness and sterility within a cleanroom environment is vital for ensuring the quality and integrity of sensitive products or processes. Thorough validation protocols are critical in confirming that a cleanroom consistently meets its predefined performance standards. This involves performing a series of tests and eva

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 critical step in establishing the suitability of a cleanroom for its intended application. This rigorous process involves a systematic analysis of the cleanroom's design to ensure it meets all relevant requirements and standards. DQ activities typically encompass reviews of engineering drawings, simulations, an