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Displaying 1 to 16 (of 16 products) Result Pages:  1 
    Product Name+   Price 
       $0.00 
    510(k) Process for Medical Devices   $1,095.00 
    Auditor/Lead Auditor Training for ISO 13485   $1,995.00 
    CAPA Programs for the Medical Device Industry   $1,095.00 
    CE Marking, EU Directives, and Guidance Documents   $1,095.00 
    Design Control Concepts and Implementation   $1,095.00 
    FDA's Quality System Inspection Technique (QSIT)   $595.00 
    Internal Auditor Training for ISO 13485   $1,195.00 
    Process Validation Principles and Protocols   $1,645.00 
    Purchasing Controls: Outsourcing and Supply Chain Management   $1,095.00 
    Risk Management and Analysis for Medical Devices   $1,095.00 
    Sterilization of Medical Devices   $1,095.00 
    Understanding an ISO 13485 Quality Management System   $1,095.00 
    Understanding FDA's Med Dev QSR and Understanding an ISO 13485 QMS and FDA's Quality System Inspection Technique-ZFF   $2,590.00 
    Understanding FDA's Medical Device Quality System Regulation   $1,095.00 
    Using Lean Six Sigma to Support FDA's PAT Initiative   $995.00 
Displaying 1 to 16 (of 16 products) Result Pages:  1 
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