ISO 13485 Standard For Medical Devices- From A to Z [2024]
Become an expert in Quality Management system and learn ISO 13485 directly from the standard guidelines.
Ratings 3.87 / 5.00
![ISO 13485 Standard For Medical Devices- From A to Z [2024]](https://img-c.udemycdn.com/course/750x422/5354746_8c7c_3.jpg "ISO 13485 Standard For Medical Devices- From A to Z [2024]")
What You Will Learn!
- Comprehensive course on the ISO 13485 standard for medical device quality management systems
- Provides a thorough understanding of the requirements and best practices for implementing and maintaining an ISO 13485 compliant quality management system
- 3-hour course covers each section and subsection of the standard, from beginner to advanced levels
- Topics covered include: 1) Scope and application of the standard 2) Quality management system requirements 3) Management responsibility 4) Resource management..
- By the end of the course, participants will have the knowledge and skills necessary to effectively implement and maintain an ISO 13485 compliant QMS system
Description
This comprehensive course on the ISO 13485 standard for medical device quality management systems is designed to provide participants with a thorough understanding of the requirements and best practices for implementing and maintaining an ISO 13485 compliant quality management system. Over the course of 3 hours, participants will be guided through each section and subsection of the standard, from beginner to advanced levels.
The ISO 13485 standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. This course will cover the scope and application of the standard, as well as the specific requirements for a quality management system that meets the standard.
Participants will learn about management responsibility, including the importance of top management commitment to the quality management system and the need for effective communication within the organization. The course will also cover resource management, including the provision of resources necessary to implement and maintain the quality management system, as well as the training and competence of personnel.
The product realization section of the course will cover topics such as planning of product realization, customer-related processes, design and development, purchasing, production and service provision, and control of monitoring and measuring equipment. Participants will also learn about measurement, analysis and improvement, including monitoring and measurement of processes and products, control of nonconforming product, analysis of data, and continual improvement.
By the end of the course, participants will have a thorough understanding of the requirements and best practices for implementing and maintaining an ISO 13485 compliant quality management system. They will have the knowledge and skills necessary to effectively implement and maintain a quality management system that meets the requirements of the ISO 13485 standard.
Who Should Attend!
- Medical Device Industry Professional Looking to Learn about ISO 13485 standard or seasoned professionals looking to refresh their skills.