Health Canada citation
Section 110 - adverse recipient reactions
Health Canada inspection citation · Blood Regulations (SOR/2013-178)
Key facts
| Requirement | Section 110 - adverse recipient reactions |
|---|---|
| Regulation | Blood Regulations (SOR/2013-178) |
| Example observations (excerpt) | the establishment had reason to believe that a recipient had an unexpected or serious adverse reaction but did not take all required actions. the establishment had reason to believe that a recipient had an unexpected or serious reaction but did not immediately notify all the required establishments. |
At a glance
- 1–9 Health Canada inspections citing this requirement
- No Among the 20 most-cited Health Canada requirements
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Health Canada regulation sections cited in inspections
Health Canada inspection reports cite the section of the Food and Drug Regulations, Medical Devices Regulations or Blood Regulations behind each observation. This page counts the published inspections that cite the requirement.
Source: Health Canada, Drug and Health Product Inspections; citation counts by Orca1. Contains information licensed under the Open Government Licence – Canada
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