With the NKF’s dedication to best practices, all the dialysis machines’ dialysate fluid parameters are tested two times a week using in-house electrolyte analyser.
All its dialysis centres have been upgraded from their previous ISO 9002 certification to ISO 9001:2000 certification in 2003.
All the medical equipment goes through strict evaluation by various committees. The evaluation, tender and finance committee assess based on the procurement value while the equipment performance and its quality will then be evaluated by our medical, nursing and biomedical engineering teams. All equipment must be approved by the USA Food and Drug Administration / European Standards (CE) and HSA. They meet or exceed IEC (International Electro technical Commission) 601-1 safety guidelines and the manufactures must have a valid of Certificate of Compliance (ISO 900 or its equivalent) for their production facilities.