The ISO 13485 Internal Auditor - 3 Days course is designed to provide a comprehensive understanding of the internal auditing process for medical device quality management systems. This intensive program covers the essentials of auditing and equips you with practical skills to audit and assess organizations for ISO 13485 compliance. Whether you’re new to internal auditing or looking to enhance your skills, this course will help you become an effective internal auditor for medical devices.

Course Outline: What You’ll Learn in 3 Days

In just three days, this course covers the following key areas:

• Introduction to ISO 13485 and its relevance to the medical device industry
• Key concepts and terminology used in internal auditing
• Audit planning, preparation, and conducting effective audits
• Identifying non-conformities and developing corrective actions
• Closing audits and ensuring compliance with ISO 13485 standards

Intensive Training for Practical Application

Our 3-day course is designed to offer both theoretical knowledge and practical experience. Through case studies, role-playing, and interactive exercises, you will gain hands-on experience in performing audits. The course is designed to simulate real-world auditing situations, helping you build confidence and competence as an internal auditor for ISO 13485.

Course Delivery and Certification

The course is delivered by certified and experienced trainers who have a deep understanding of ISO 13485. Upon successful completion, you will receive a certificate that qualifies you as an ISO 13485 Internal Auditor, ready to take on auditing roles within medical device organizations.

Conclusion

If you're looking to enhance your auditing skills in the medical device sector, the ISO 13485 Internal Auditor - 3 Days course is an excellent opportunity. This course will provide you with the skills and knowledge needed to conduct effective audits and ensure compliance with ISO 13485 standards. For more details and to register, visit QMII's registration page.