Implementing ISO 13485 Training Course

Put quality first with our Implementing ISO 13485:2003 Training Course – make sure your medical devices are internationally recognised and meet legal and customer requirements.

“While quality has always been our number one priority, we now have a more systematic approach to the way it is managed.”

This course shows you how to put in place a quality management system in line with ISO 13485:2003, paving the way to accreditation. ISO 13485 is a clear mark of your commitment to quality and applies to every aspect of medical devices from design to development, production and servicing. You will learn step by step how to plan, develop and implement a quality management system. Working with our experts, you will take away the skills to achieve and maintain best quality management practice, gain customer confidence and quicker access to market.

Learning objectives

• Understand the structure and scope of the ISO 13485 quality management system
• Learn how this applies to your organisation in relation to compliance
• Be able to plan and implement an ISO 13485 quality management system
• Lead processes, develop policies and measure progress
• Prepare for ISO 13485 certification
• Boost professional recognition and CPD.

Benefits of attending this course?

• Take the first steps towards ISO 13485 accreditation
• Understand how you can better meet customer and regulatory requirements
• Find ways to increase efficiency and cost savings through quality management
• Monitor supply chains to achieve continuous improvement
• Develop safe and effective medical devices
• Motivate employees through CPD.