ISO 13485

Product Preservation Record

Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.

Fully Customizable Audit Ready Instant Download
Standard
ISO 13485
Document Type
Records
Format
DOCX
Language
English
Tags
ISO 13485, Medical Devices, Records

A Product Preservation Record showing that product conformity was maintained during processing, storage, handling and distribution, covering preservation requirements, storage condition monitoring, shelf life and FEFO control at shipment, stock checks and periodic warehouse inspections. It comes with a completed worked example.

What's Inside

  • Purpose and Summary
  • Preservation Requirements
  • Storage Conditions Monitoring
  • Shelf Life and FEFO at Shipment
  • Stock on Hand Check
  • Monthly Warehouse Inspections
  • Review and sign-off section

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