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Training for ISO 13485 - Medical Device Industry

SAI Global's comprehensive ISO 13485 and regulatory support program for the Medical Device Industry enables your organization to implement an effective ISO 13485 quality management system and meet domestic and international regulations for medical device, while achieving overall business improvement. 


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Online Root Cause Analysis 

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Online Lead Auditor Training  

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ISO 13485 Training Courses
Implementing CoursesInfoAgendaPublicIn-HousePrice
Corrective and Preventive Action (CAPA) for FDA Regulated Industries Course  


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Risk Management ISO 31000 Foundation 


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