Transitioning to ISO 13485:2003 Overview – Virtual Course

Who Should Attend

Quality assurance, engineers, ISO coordinators and other personnel responsible for transitioning a firm's existing ISO 13485 quality management system.

Learning Outcomes

• Review the requirements of ISO 13485:2003
• Understand the new responsibilities of top management
• Discover the importance of quality objectives and process approach to business
• Examine regulatory industry changes
• Learn transition steps
• Learn about audit program changes

Market Focus: Manufacturing

Related ASQ Bodies of Knowledge:

Medical Device auditing, ISO 13485

Instructor(s):

Rand Winters

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