category iso 13485 online coursesISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is an International Organization for Standardization (ISO) standard published for the first time in 1996; it represents the requirements for a comprehensive quality management system for the design and manufacture of medical devices.
ISO 13485:2016 Overview & Transition, Internal Auditor Issues

An audit always finds areas for improvement. 

Effective Corrective Actions address what is important.  Also just as important is HOW they are presented.  Opportunities are usually positive and when Effective Corrective Actions are presented in a positive manner, the probability for success increases.

This short course covers the basic requirements and the process to follow.
Duration: 240 days
Price: $895.00