ISO 13485 is an ISO standard that establishes requ..

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ISO 13485 is an ISO standard that establishes requirements for medical device manufacturer’s quality management systems. On January 1, 2016, ISO released the newest version of this standard, ISO 13485:2016. ISO 13485 training courses can help companies better understand and apply quality management criteria in the design, production, installation, and servicing of medical equipment.
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ISO 13485 Training |ISO 13485 Auditor Training - IAS Canada

ISO 13485 training enables individuals to understand the requirements of a quality management system for medical devices to ensure safe products.

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ISO 13485 Training |ISO 13485 Auditor Training - IAS Canada

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