Health Canada citation
C.05.012 - records
Health Canada inspection citation · Food and Drug Regulations (C.R.C., c. 870), Part C
Key facts
| Requirement | C.05.012 - records |
|---|---|
| Regulation | Food and Drug Regulations (C.R.C., c. 870), Part C |
| Example observations (excerpt) | deficiencies were noted in the completeness, accuracy or availability of the required records. medical care and/or medical decisions for the clinical trial were not under the supervision of the qualified investigator at the clinical trial site. the sponsor did not implement systems and procedures to… |
At a glance
- 100–999 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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