13485 P-820 Post Production Feedback

Procedure - Post Production Feedback - Includes forms: F-821-001 Customer Satisfaction Survey and Analysis, F-852-001 Corrective/Preventive Action Request, F-425-001 Quality Records table.

Format: MS Word
Language: English
Product Type: Digital
Provider: 13485 Store

Price: $35.00
Product Details

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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