Regulatory Requirements Register
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
- Register
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Register
ISO 13485:2016 requires your organisation to identify applicable regulatory requirements, document its regulatory roles (clause 4.1.1), include regulatory requirements in QMS documentation (clause 4.2.1 e)), and review new or revised requirements at Management Review (clause 5.6.2 l)).
What's Inside
- Regulatory Roles Summary
- Regulatory Requirements
- International / QMS
- European Union
- United States
- Singapore
- Malaysia
- Other Legal Requirements
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clauses 4.1.1, 4.2.1 and 5.6.2. 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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