ISO 13485
Internal Audit Procedure
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
- Procedure
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Procedure
This procedure defines how your organisation plans, conducts, records and follows up internal audits, as required by ISO 13485:2016 clause 8.2.4.
What's Inside
- Audit Programme
- Risk-Based Audit Frequency
- Auditor Selection, Competence and Objectivity
- Audit Preparation
- Conducting the Audit
- Classification of Findings
- Closing Meeting
- Audit Report
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clause 8.2.4. 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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