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
Price:
$39.00
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.
Customers Also Bought
- IMS Small Business Package (9001:2015 QMS+14001:2015 EMS+45001:2018 OHSMS+50001:2018 EnMS)
Price: $1897 BUY NOW - IMS All-in-One Documentation and Training Package (9001:2015 QMS+14001:2015 EMS+45001:2018 OHSMS+50001:2018 EnMS)
Price: $2497 BUY NOW - Integrating 9001:2015-45001:2018 PowerPoint
Price: $149 BUY NOW - IMS Small Business Package (9001:2015 QMS+45001:2018 OHSMS)
Price: $997 BUY NOW - IMS All-in-One Documentation and Training Package (9001:2015 QMS+45001:2018 OHSMS)
Price: $1497 BUY NOW - Checklist for ISO 14001:2015 - Environmental Management Systems - Requirements with Guidance for Use
Price: $330 BUY NOW
You Recently Viewed
