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  2. Enhance medical device quality management with our ISO 13485 training courses. Learn ISO 13485 standards and ensure compliance. Enroll now.

  3. Learn how to apply quality management standards for the medical device manufacturing industry with ASQ's ISO 13485 training courses. Find out how to become a lead auditor and access online and in-person classes.

  4. Develop the skills you need to lead a successful medical device audit in this ISO 13485 lead auditor training course. Specifically designed to meet the needs of the medical device industry, this four-day class prepares medical device lead auditors for real-life situations via hands-on workshops.

  5. Module 1: Introduction to ISO 13485:2016. Introduction. What is ISO 13485:2016? Importance of ISO 13485. Module 2: Overview of ISO 13485:2016 Requirements. Requirements of ISO 13485:2016. General Requirements. Documentation requirements. Management Responsibility. Resources. Product Realization. Infrastructure. Risk Management.

  6. Develop skills to identify, assess, and manage risks associated with medical devices. Expand your knowledge under the guidance of world-class training instructors. Validate your skills with the ISO 13485 Training in the United States. View courses Inquire now.

  7. This two-hour course provides in-depth instruction and expert clarification of ISO 13485:2016, the standard that serves as a basis for many medical device QMS regulations around the globe.

  8. Take DEKRA's ISO 13485:2016 4-Day Lead Auditor Training, certified by Exemplar Global, to learn how to audit a Quality Management System with a focus on the Medical Device industry.

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  4. Become an ISO 13485 Expert with Award-Winning ISO 13485 Training Courses. Exams Included. Global Market Leader of ISO Certification, High Quality ISO 13485 Certification Courses!

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