ComplianceOnline

13485 P-820 Post Production Feedback


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.

Best Sellers
You Recently Viewed
    Loading
Loading...