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ISO 13485 standards for quality management system on medical devices Toronto

  Marketing & Advertising

ISO 13485 is an international standard that specifies requirements for a quality management system (QMS) for organizations involved in the design, ISO Medical Devices Quality Management System development, production, installation, and servicing of medical devices.

In the medical device industry, compliance with ISO Consultants in Canada standards is crucial for demonstrating the ability to provide medical devices and related services that consistently meet customer and regulatory requirements.






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