Customer Feedback Register
Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.
- Standard
- ISO 13485
- Document Type
- Register
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Register
This register records feedback from customers, users and the market. ISO 13485:2016 clause 8.2.1 requires your organisation to gather and monitor information on whether it has met customer requirements, to document the methods for obtaining and using this information, and to establish a feedback process that provides early warning of quality problems and input into corrective and preventive action.
What's Inside
- Feedback Sources and Methods
- Feedback Register
- Use of Feedback
- Customer Satisfaction Survey 2027 (FB-27-017)
- Analysis
- Review
- Review and sign-off section
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clause 8.2.1. It fits with the rest of the QEHS Vault ISO 13485 document set.
Format
Supplied as a fully editable Microsoft Word (.docx) file. Add your organisation’s name, logo and details, then use it straight away. Instant download after purchase.
Key Benefits
- Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements
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