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› 13485 P-820 Post Production Feedback
13485 P-820 Post Production Feedback
Format: MS Word
Language: English
Product Type: Digital
Provider: 13485 Store
Language: English
Product Type: Digital
Provider: 13485 Store
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ISO 13485:2016 Procedure - Post Production Feedback - defines the process whereby post production experiences are evaluated and acted upon. Describes a documented feedback system to collect and review information about medical devices in post-production phases. The information is evaluated for possible relevance to safety and device efficacy.
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