ISO 13485:2016 Auditor Training

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ISO 13485:2016 is an international standard that establishes the requirements for a quality management system specific to the medical devices industry. It specifies requirements for a quality management system, and how to demonstrate compliance to meet customer and applicable regulatory requirements. ISO 13485 is designed to be used by organizations involved in the design, production, installation, and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes.  Estimated to take up to 15-hours to complete.

Objectives

By participating in this online course, you will be able to:

• Explain the high level requirements and intent of this international standard
• Explain how the requirements can be interpreted/should be implemented in various industries
• Identify the requirements for managing an organization’s QMS in compliance with ISO 13485:2016
• Interpret how the requirements can be interpreted/should be implemented within an organization
• Assume a productive role in an audit of your organization’s quality management system as outlined in ISO 13485 and ISO 19011

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