The creation, maintenance, processing, and/or review of laboratory data was inadequate.
Inspection Record
Contract Pharmaceuticals Limited Canada — Health Canada Inspection Findings
View the regulator's official source The source document is always the basis for judgement.
Findings
The temperature and/or humidity control was inadequate.
The handling of standard operating procedures for good manufacturing practices was inadequate. The traceability, legibility, documentation, formatting, and/or the accuracy of records was inadequate.
The calibration, inspection, and/or qualification of the equipment, including computerized systems, was inadequate.
The handling and/or storage of samples was inadequate for raw materials, drugs being processed, bulk drugs, and/or finished products.
The ongoing stability program for a drug was inadequate.
The investigation, handling, and/or reporting of test results that were out-of-specification was inadequate.
The change control system was inadequate for ensuring changes are properly documented, evaluated, and/or approved.
The design, equipment, and/or maintenance of the testing laboratory was inadequate.
Investigations into deviations, reports, and/or follow-up actions were inadequate.
The monitoring procedures for microbial and/or environmental conditions were inadequate.
The controls were inadequate for creating, modifying, reviewing, storing, and/or retrieving records.
About this record
Extracted automatically from the document of the Health Canada inspection on 2026-02-09. 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.
