Health Canada citation

MDR s.80(2) - authorization and records

Health Canada inspection citation · Medical Devices Regulations (SOR/98-282)

Key facts

Requirement MDR s.80(2) - authorization and records
Regulation Medical Devices Regulations (SOR/98-282)
Example observations (excerpt) risk 2: the company could not provide the required records to support the investigational testing authorization from health canada. the company sold a device for investigational testing without authorization from health canada.

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

Browse all Health Canada regulation sections cited in inspections