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13485:2016 Medical Devices Quality Management Systems

ISO 13485:2016 is a globally recognized standard that specifies requirements for a quality management system (QMS) specifically for organizations involved in the design, production, installation, and servicing of medical devices. It focuses on maintaining consistent quality and regulatory compliance, ensuring that products meet customer and applicable regulatory requirements. The standard emphasizes risk management, process improvement, and documentation, fostering a culture of continuous enhancement in the medical device sector.

LICQual ISO 13485:2016 Medical Devices Quality Management Systems
ISO Lead Auditor | LICQual

LICQual ISO 13485:2016 Medical Devices Quality Management Systems

The LICQual ISO 13485:2016 Medical Devices Quality Management Systems (QMS) course offers essential training designed for professionals in the healthcare and…

Read More LICQual ISO 13485:2016 Medical Devices Quality Management SystemsContinue

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  • Home
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  • Courses
    • OTHM
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