ISO 13485
Nonconformity and Corrective Action Procedure
Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.
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- Standard
- ISO 13485
- Document Type
- Procedure
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Procedure
This procedure defines how your organisation identifies and controls nonconforming product, and how it takes corrective and preventive action.
What's Inside
- Control of Nonconforming Product
- Identification and Segregation
- Documentation
- Evaluation
- Actions Before Delivery
- Actions After Delivery
- Rework
- Closure and Trending of NCRs
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clause 8.5.2. 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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