![]() ![]() This document replaces the previous version based on the previous versions of Health Canada guidance documents.Ģ. It describes the auditing procedure for quality management systems according to ISO 13485 under the Canadian Medical Devices Conformity Assessment System (CMDCAS) based on the Health Canada guidance documents GD 207 (November 2007) and GD 210 (January 2007). Purpose This checklist is a supplement to Supplement Assessor Guideline MDD and CMDCAS 780E1, and the Checklist for the Assessment in Accordance with the Standards ISO 13485 etc. Supplement-Checklist for the assessment in accordance with ISO 13485 under CMDCAS 1.
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