# Adverse incidents: in vitro diagnostic (IVD) blood glucose meters

Source: https://www.keypedia.com/records/uk_mhra_guidance/uk-mhra/fea583eb-586d-463e-95cd-e1d69aa6e5fb
Type: Guidance
Published: January 26, 2015
Updated: January 15, 2025

> Device-specific guidance for manufacturers on reporting adverse incidents under the vigilance system.

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## Content

Guidance for manufacturers reporting adverse incidents involving on IVD blood glucose monitors under the vigilance system. To be read in conjunction with the guidelines on post market surveillance .

## Attachments

- [Device-specific vigilance guidance:  in vitro diagnostic (IVD) blood glucose monitors, covering point of care testing and home use](/government/publications/adverse-incidents-in-vitro-diagnostic-ivd-blood-glucose-meters/device-specific-vigilance-guidance-in-vitro-diagnostic-ivd-blood-glucose-monitors-covering-point-of-care-testing-and-home-use)