ISO 13485
Regulatory Reporting 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 notifies regulatory authorities of complaints and events that meet the reporting criteria of the applicable regulations, and how it issues advisory notices (field safety notices) and carries out field actions.
What's Inside
- Procedure — Adverse Event Reporting
- Identification of Potentially Reportable Events
- Reportability Assessment
- Reporting Timelines
- Preparation and Submission of Reports
- Investigation, Follow-up and Final Reports
- Periodic and Trend Reporting
- Closure of Vigilance Files
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clause 8.2.3. 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
Reviews
There are no reviews yet.