• Accredited Training: Gain expertise in auditing Medical Device Quality Management Systems (MD QMS) against ISO 13485:2016 with our IRCA/CQI Accredited ISO 13485 Lead Auditor Training.

  • Course Objectives: Learn to understand the purpose of MD QMS, interact with regulatory authorities, grasp quality management standards, and recognize the business benefits of QMS. Develop skills in planning, conducting, and reporting QMS audits in alignment with ISO 19011 and ISO 17021.

  • Comprehensive Curriculum: Cover essential topics including process-based MD QMS, accreditation, certification, audit principles, and audit stages. Master audit preparation, checklist development, on-site audit execution, and post-audit activities.

  • Expert Instruction: Benefit from expert guidance to comprehend roles and responsibilities of auditors, ensuring conformity with ISO 13485 and relevant regulatory documents.

For detailed information on our IRCA/CQI Accredited ISO 13485 Lead Auditor Training, Fill in the form to know more. Elevate your auditing skills and enhance your career in the medical devices industry.

ISO 13485 LEAD AUDITOR TRAINING COURSE

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