Medical Device Industry Courses : Axeon

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> ISO 17025

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> ISO 13485 Medical Devices

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Courses

Medical Device Industry Courses

$1895.00 5 Day (36 hr) RABQSA Certified Lead Auditor with ISO 13485 Medical Device Focus - Call for group/membership discounts or onsite pricing Read course agenda This course has been specifically designed to meet the needs of the Medical Device Industry. Those responsible for planning and scheduling an audit program for ISO 13485 and those who must perform audits to ISO 13485, Quality Assurance Managers, Quality Assurance Professionals, ISO Project Managers, ISO Project Team Members, Compliance Managers, Regulatory Personnel or anyone desiring an in-depth understanding of the ISO 13485 Audit Process.

This course is certified in the RABQSA Certification Program (AQS Management), and meets the training portion of the requirements for certification of individual Quality Systems Provisional Auditors, Quality Systems Auditors, and Quality Systems Lead Auditors.

$1195.00 3 Day (24 hr) RABQSA Certified Internal Auditor Course with ISO 13485 Medical Device Focus - Call for group/membership discounts or onsite pricing Those responsible for planning and scheduling an internal audit program for ISO 13485 and those who must perform audits to ISO 13485, Quality Assurance Managers, Quality Assurance professionals, ISO Project Managers, ISO Project Team Members or anyone designing in in-depth understanding of the ISO 13485 Audit Process.

This course is certified in the RABQSA Certification Program (AQS Management) and meets the training portion of the requirements for certification of individual Quality Management System Internal Auditors.

$995.00 2 Day ISO 13485 Project Management Transition- Implementation - Call for group/membership discounts or onsite pricing Those responsible for planning, implementing, and ensuring the success of implementation of ISO 13485:2003. This includes Quality professionals, Project Managers and Team Members, Quality Auditors, Quality Consultants, or anyone who wants a clear understanding of the requirements of the ISO 13485 Medical Device standard.