Reporting adverse incidents: intraocular lenses
- Medicines and Healthcare products Regulatory Agency
- Part of:
- Medical devices: guidance for manufacturers on vigilance, Patient safety, Medical devices regulation and safety, and Vigilance, safety alerts and guidance
- First published:
- 1 June 2009
For manufacturers reporting adverse incidents with intraocular lenses under the European vigilance system.
PDF, 52.3KB, 2 pages
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Published: 1 June 2009