Internal Auditor Training Program Based on ISO 13485 Standard (Medical Device)
9th - 10th Oct 2020: Internal Auditor Training Program Based on ISO 13485:2016 | 2 Days
30th - 31st Oct 2020: Internal Auditor Training Program Based on ISO 13485:2016 | 2 Days
ISO 13485 – Medical Device – Quality Management Systems –Requirements for regulatory purpose – address the development, implementation and maintenance of quality management system intended for use by medical device manufacturers, developers, and suppliers. The standard details the requirement for quality management systems, to meet customer requirement and allows the incorporation of applicable regulatory requirements within an organization’s quality management system
Module 1 – ISO 13485:2016 Requirements (Day 1)
This topic will enable participants to understand the requirements of ISO 13485:2016, a standalone Quality Management Systems standard for Medical Device manufacturers and mandatory while fulfilling the regulatory compliance.
Module 2 – Auditing Techniques (Day 2)
This topic will provide knowledge to participants on the Auditing Techniques like Auditing Concepts, Audit Planning, Audit Execution and Audit Reporting, based on ISO 19011 Standard. This will be followed by a written examination, for evaluation purposes.
Preferred to have basic knowledge of Quality Management System - ISO 13485 Standards and / or experience if medical device operations.
Participants will be assessed through a 50 marks written examination (open book) at
the end of the course. Minimum passing % criteria: 70%.
Participants who score 70% and above in the written examination will be issued a TÜV SÜD South Asia’s internal auditor certificate. Unsuccessful candidates will be issued a certificate of attendance.
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Bosnia and Herzegovina