Comparison analysis of nonconformities and strategy of change version for ISO 15189:2012 and ISO 15189:2022
	    		
		   		
		   			
		   		
	    	
    	 
    	10.13602/j.cnki.jcls.2024.04.14
   		
        
        	
        		- VernacularTitle:ISO 15189:2012和ISO 15189:2022的不符合对照分析及换版策略
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jing HE
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
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			        		Changai HU
			        		
			        		;
		        		
		        		
		        		
			        		Dagan YANG
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. 绍兴文理学院附属医院检验科,浙江绍兴 312000;浙江大学医学院附属第一医院检验科,杭州 310003
			        		
		        		
	        		
        		 
        	
        	
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		medical laboratory;
			        		
			        		
			        		
				        		accreditation;
			        		
			        		
			        		
				        		nonconformity;
			        		
			        		
			        		
				        		risk management;
			        		
			        		
			        		
				        		ISO 15189:2022
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Clinical Laboratory Science
	            		
	            		 2024;42(4):304-307
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
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		        	Abstract:
			       	
			       		
				        
				        	Objective To analyze nonconformities between 2012 and 2022 version of ISO 15189,and provide strategies of transitioning to new standard for laboratories.Methods A total of 522 nonconformities from 32 on-site audits in 24 laboratories against ISO 15189:2012 were collected and mapped them to the relevant clauses of ISO 15189:2022.Strategies for transitioning ISO 15189 to new version were explored based on the standard requirements,literature review and current laboratory practices.Results On average,16 noncon-formities(range from 8 to 31)were identified in every on-site audit.Most of them were related to ISO 15189:2022 clauses 7.3 Exami-nation Processes(165 nonconformities).The others were clause 6.5 Equipment Calibration and Metrological Traceability(43)and clause 6.6 Reagents and Consumables(40).Relatively fewer nonconformities involved new/enhanced requirements,such as risk man-agement,patient-related processes and point-of-care testing.Conclusion The main nonconformities in ISO 15189:2022 predominantly involved in the link of examination processes.It should be suggested that the laboratories strengthen the management in this area by a-dopting digital/intelligent technologies in order to smoothly implement the requirements of the new version of ISO 15189:2022 standard.A comprehensive strategy,including incorporating training,gap analysis,document revision,implementation involved in all staff,stringent risk management and continuous improvement should be recommended to ensure successful transition progress for replacement of ISO 15189:2022.