Product Preservation Procedure
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
- Procedure
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Procedure
This procedure defines how your organisation preserves the conformity of product to requirements during processing, storage, handling and distribution, as required by ISO 13485:2016 clause 7.5.11. Preservation applies to the constituent parts of a medical device as well as to the finished device.
What's Inside
- Determining Preservation Requirements
- Packaging and Shipping Containers
- Preservation During Processing
- Handling
- Storage
- Special Conditions
- Distribution and Transport
- Damage and Excursions
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clause 7.5.11. 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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