This comprehensive course provides a strong foundation for understanding the Quality Management System for medical devices and ISO 13485.
It will give you insights into the key requirements for establishing and maintaining compliant systems and processes.
Through a step-by-step approach, you will expertly be guided through the standards, with a primary focus on ISO 13485.
Additionally, you will gain an overview of essential standards and regulations, including MDSAP, EU MDR, and QSR.
Furthermore, the course will provide you with insight and understanding of the structure of effective Quality Management Systems, as well as the key requirements needed for establishing and maintaining a compliant system and processes.
You will also be presented (high level) with critical elements of the quality management system, such as design control (product development), manufacturing, validation, management responsibilities, handling of resources, internal audits, change control, post-market surveillance, and CAPA management, to gain an overall understanding of the backbone of the QMS system.
To sum up: after the course you will effectively be able to contribute to compliant systems, elevate the decision-making, and play a pivotal role in your organisation's operational excellence. You will be able to navigate complex standards, ensure compliance, and become catalysts for quality enhancement in the dynamic medical device industry.
The course language is English.
At the course you will meet:
Naram El-Shamary, Managing Partner, ImproveMatic – Quality by Simplicity
