ISO 13485
Interested Parties Register
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
- Register
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Register
This register identifies the interested parties relevant to the Quality Management System (QMS) of your organisation, their needs and expectations, and which of those become QMS requirements (compliance obligations).
What's Inside
- Interested Parties, Needs and Expectations
- QMS Requirements and How They Are Addressed
- Communication with Key Interested Parties
- Review Record
- Review and sign-off section
ISO 13485 Alignment
Written to support ISO 13485:2016 Medical Devices Quality Management System requirements. 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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