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Displaying 1 to 15 (of 15 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 - L2KF   $1,995.00 
    CAPA Programs for the Medical Device Industry - CAPF   $1,095.00 
    CE Marking, EU Directives, and Guidance Documents - DIRF   $1,095.00 
    Design Control Concepts and Implementation - DCAF   $1,095.00 
    FDA's Quality System Inspection Technique (QSIT) - MSFF   $595.00 
    Internal Auditor Training for ISO 13485 - I2KF   $1,195.00 
    Process Validation Principles and Protocols - PV3F   $1,095.00 
    Risk Management and Analysis for Medical Devices - FMEF   $1,095.00 
    Sterilization of Medical Devices - STEF   $1,095.00 
    Understanding an ISO 13485 Quality Management System - QASF   $1,095.00 
    Understanding FDA's Med Dev QSR and Understanding an ISO 13485 QMS and FDA's Quality System Inspection Technique-ZFIF   $2,590.00 
    Understanding FDA's Medical Device Quality System Regulation - MGMF   $1,095.00 
    Using Lean Six Sigma to Support FDA's PAT Initiative - PATP   $995.00 
Displaying 1 to 15 (of 15 products) Result Pages:  1 
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