Health Canada citation
C.02.020 - records
Health Canada inspection citation · Food and Drug Regulations (C.R.C., c. 870), Part C
Key facts
| Requirement | C.02.020 - records |
|---|---|
| Regulation | Food and Drug Regulations (C.R.C., c. 870), Part C |
| Example observations (excerpt) | a documentation system involving a “certificate of manufacture” was used by an importer of drugs from non-mra countries, but complete batch documentation was not obtained by the importer at least once per year per drug. complete traceability of api distributed was not maintained. computerized… |
At a glance
- 1,000+ Health Canada inspections citing this requirement
- Yes 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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