ISO 13485 Foundation – Medical Devices

What is ISO 13485? As an international standard, ISO 13485 determines the requirements for the medical devices industry. This standard was established to be used by companies during the life cycle of medical devices, from the production to post-production, including decommission and disposal. However, ISO 13485 can also be operated by other parties such as certification bodies which can assist in the certification processes. ISO 13485 serves as a tool for organizations to develop and retain their processes efficiently. Organizations that are striving for continuous improvement will benefit from this standard by being able to provide safe and competent medical devices and achieve the trust of customers.

Why is Medical Devices Quality Management System important for you?

Being an ISO 13485 certified professional imposes your determination to offer qualitative products and services to your company and/or clients. Attaining the necessary knowledge and skills to operate an ISO 13485 framework demonstrates your commitment to helping your company ensure continuous improvement and better work processes. It also indicates that you understand the importance of the safety and performance of medical devices and how a medical devices quality management system can assure just that, consequently leading to customer satisfaction. Similarly, it can introduce you to new opportunities, such as working for large companies that offer quality products and services. These companies will value your knowledge and expertise on this standard, while enabling you to maximize your earning potential.

Learning objectives

• Understand the concepts, approaches, methods and techniques used to implement a Medical Devices Quality Management System (MDQMS)
• Understand the basic elements of a Medical Devices Quality Management System (MDQMS)

Benefits of ISO 13485 Medical Devices Quality Management System

By becoming an ISO 13485 certified professional, you will be able to:

• Increase the number of job opportunities
• Create new business connections
• Gain competitive advantage
• Increase effectiveness and lower costs
• Offer expertise on improving work processes
• Offer safer and more efficient medical devices
• Increase customer satisfaction

Why should you attend?

Who should attend?

• Individuals interested in Medical Devices Quality Management
• Individuals seeking to gain knowledge about the main processes of Medical Devices Quality Management System (MDQMS)

Course Agenda : Introduction to Medical Devices Quality Management System (MDQMS) concepts as required by ISO 13485

• Training material containing over 100 pages of information and practical examples will be distributed
• A participation certification of 7 CPD (Continuing Professional Development) credits will be issued

Related FEE

• International Student Training Fee 300USD | 1125 SAR | 1125 AED
• PECB Certification Exam Fee : 500 USD (Not Included in Training Fee)

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