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ISO 13485
- Date: March 29, 2011
 - Source: Admin
 
Compliance Webinars | Virtual Seminars for Professionals
REQUIREMENTS FOR ISO 13485
Systemic Requirements
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             Establish a Quality System for Medical Devices  | 
            
            
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             Document Your Medical Device Quality System  | 
            
            
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Management Requirements
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             Support Quality  | 
            
            
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             Focus on Customers  | 
            
            
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             Establish a Quality Policy  | 
            
            
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             Perform Quality Planning  | 
            
            
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             Control the Quality Management System  | 
            
            
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             Carry Out Management Reviews  | 
            
            
 
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Resource Requirements
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             Provide Quality Resources  | 
            
             · Identify quality management system resource requirements · Provide quality management system resources  | 
        
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             Provide Quality Personnel  | 
            
             · Use competent personnel · Support competence  | 
        
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             Provide Quality Infrastructure  | 
            
             · Identify infrastructure needs. · Provide needed infrastructure · Maintain your infrastructure  | 
        
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             Provide Quality Environment  | 
            
             · Identify needed work environment · Implement needed work environment · Manage needed work environment  | 
        
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