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Earlier capture
Quality Systems ISO 13485 - Canada.ca
Apr 18, 2025
legacy-hc-2025-04-21
ID 168708
Later capture
Quality Systems ISO 13485 - Canada.ca
Jan 2, 2026
hc-20260101
ID 429021
updated2 sections changed
2 sections changed0 added0 removed+0 / -13 linesChange ratio: 13%
--- +++ @@ -17,18 +17,6 @@ The following Training Modules summarize the contents of the Study Guide GD211: Guidance on the content of quality management system audit reports and are available as a convenience to the user. The Training Modules are available in Microsoft PowerPoint and Portable Document Format as an alternate format to the Study Guide.-GD211 Training, Module 1 - Introduction-[2011-12-07]-GD211 Training, Module 2 - Information about the manufacturer-[2011-12-07]-GD211 Training, Module 3 - Information about the audit-[2011-12-07]-GD211 Training, Module 4 - Audit Findings-[2011-12-07]-GD211 Training, Module 5 - Conclusions-[2011-12-07]-GD211 Training, Summary-[2011-12-07] CDRH Learn Portal - Online video training on GD211 Guidance Document GD211: Guidance on the Content of Quality Management System audit reports [2011-06-08]@@ -53,5 +41,4 @@ List of registrars recognized by Health Canada (HC) under section 32.1 of the Medical Devices Regulations (MDR) [2015-01-20] Page details-Date modified: 2019-02-01