Maintaining a high level Thorough and Objective Supplier Evaluation of cleanliness and sterility within a cleanroom environment is essential for guaranteeing the quality and integrity of sensitive products or processes. Rigorous validation protocols are instrumental in demonstrating that a cleanroom consistently meets its predefined performance sta

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 essential step in establishing the suitability of a cleanroom for its intended application. This rigorous process involves a systematic assessment of the cleanroom's configuration to ensure it meets all necessary requirements and standards. DQ activities typically comprise reviews of engineering drawings, simul