ISO 13485
Document Master List
Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.
Fully Customizable
Audit Ready
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- Standard
- ISO 13485
- Document Type
- List
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, List, Medical Devices
This list identifies every controlled document of the your organisation medical device quality management system and its current revision status.
What's Inside
- Document Structure and Numbering
- Master List of Controlled Documents
- Level 1 — Manual, Policy and Scope
- Level 2 — Procedures
- Summary
- External Documents
- Cross-Reference Corrections and Duplicates
- Superseded References in the Quality Manual
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clause 4.2.4. 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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