The ongoing training of personnel was inadequate. The training of personnel in good manufacturing practices and/or the maintenance of records was inadequate.
Inspection Record
DSV Contract Logistics Inc. — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
The quality control department was not involved in all decisions for the quality of the product. The assessment to release finished products was inadequate. Documents were not available on the premises.
The ongoing stability program for a drug was inadequate.
The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate. The distribution records did not allow each drug to be traced individually.
The temperature and/or humidity control was inadequate.
The handling of standard operating procedures for good manufacturing practices was inadequate.
Senior management's ability to determine and/or provide adequate and/or appropriate resources to implement, maintain and/or improve the effectiveness of the quality management system was inadequate.
The availability or the content of the authentic certificate of analysis was inadequate.
Investigations into deviations, reports, and/or follow-up actions were inadequate.
The confirmatory tests conducted on samples before or after they were received in Canada were inadequate.
The assessment to release finished products was inadequate.
About this record
Extracted automatically from the document of the Health Canada inspection on 2025-06-11. The source is available at the link above.
This is a record of that moment. Inspection findings are usually followed by the company's response and corrective action, but this page does not know how that turned out. Do not read it as the current state; check the regulator's official announcements for the latest status.
Translation and classification are automated and may differ in nuance from the source.
