How can I monitor the effectiveness of my QMS after my medical device reaches the market? We'll discuss the procedures you need to put in place to maintain quality control of your medical equipment and QMS processes.

In this video we explain how your quality management system should function in a post-market environment to meet the demands of quality events that occur with your medical device.

This final part of the process is known as the Track phase of our 5-phase SMART QMS implementation methodology, where you will learn how to implement new QMS processes responsible for tracking the health of your medical device quality management world class. system.

You will learn 7 QMS procedures for monitoring and maintaining healthy QMS processes:
1. Corrective and Preventive Actions (CAPA)
2. Post-market monitoring and data analysis
3. Internal audit
4. Non-conformities
5. Complaints handling
6. Reporting of medical devices/reporting of adverse reactions
7. Customer feedback

This video will give you proven tactics and approaches you can use to easily set up these procedures in your world-class quality system, and best practices for leveraging each process to achieve lasting success throughout the entire life cycle of your product.

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Are you looking for an all-in-one QMS solution to increase the success of your in-market devices and integrate your quality processes with product development efforts? See how our medical device QMS software can help you: https://www.greenlight.guru/quality-management-software

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