Medical Device Process Validation - Statistical Aspects - Webinar By GlobalCompliancePanel 2012

Medical Device Process Validation - Statistical Aspects is a webinar that covers topics such as:

• The Statistical Process Model
• QMS Requirements for Process Validation
• The Process Input Parameters
• The Process Output
• Risk Management

Medical Device Process Validation - Statistical Aspects brings together Medical Device professionals including Quality Engineers, Quality Managers, Production Supervisors, Production Managers, Production Engineers, Manufacturing Engineers, Process Owners and Design Engineers.