Contemplation and Suggestion on the Medical Device Adverse Event Reporting Program
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3969/j.issn.1671-7104.2014.01.019
   		
        
        	
        		- VernacularTitle:对我国医疗器械不良事件监测系统的思考和建议
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Baodong YU
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Yingjie GUAN
			        		
			        		;
		        		
		        		
		        		
			        		Xiaomei MO
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. 山东省青岛市妇女儿童医院
			        		
		        		
	        		
        		 
        	
        	
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		medical device;
			        		
			        		
			        		
				        		adverse event;
			        		
			        		
			        		
				        		evaluation;
			        		
			        		
			        		
				        		deficiency;
			        		
			        		
			        		
				        		suggestion
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Chinese Journal of Medical Instrumentation
	            		
	            		 2014;(1):65-67
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	The number of medical device adverse events reported to national monitoring center increased greatly year by year, but the reporting system stil existed some deficiencies which resulting in confusion when fil ing the forms, especial y those selections about relationship evaluation. This paper proposed amendments about event-evaluation process according to the characteristics of medical device adverse events reported in China, in order to perform timely and effectively regulation on different types of adverse events for different purposes.