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Versions and revisions! Document control in eQMS software

June 27, 2019June 27, 2019

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#medicaldevice Article audit CAPA CAPA requirements CAPA steps Cardio Compliance DMS document control document management software employees eQMS FDA hazard Heartcare inspection ISO ISO 13485 iso13485 ISO14971 medical device Medical devices outsourced manufacturer paper-based Processes Product QMS qms manager qms software qmsWrapper quality management system Quality Manager Quality Manual RCA Regulations risk riskanalysis Risk Based risk evaluation riskmanagement risk report Root Cause Analysis Standard Traceability

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