Directives bulletin 3: European vigilance system in the UK
- Medicines and Healthcare products Regulatory Agency
- Part of:
- Regulatory guidance for medical devices, Patient safety, Medical devices regulation and safety, and Vigilance, safety alerts and guidance
- First published:
- 1 September 2008
Guidance for manufacturers on how the European vigilance system works in the UK.
PDF, 819KB, 38 pages
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See this for general guidance on how the European vigilance system operates in the UK.
You should read this guidance alongside the European Commission’s guidelines on the vigilance system for medical devices.
Published: 1 September 2008