ISO 14971:2019 Risk Management for Medical Devices: Requirements Training Course (NITTP available)

This one-day intensive course enables greater understanding of the impact that ISO 14971:2019 has on the decision-making process when manufacturing medical devices.
It helps medical device professionals understand how ISO 14971:2019 can improve their business and risk management efforts.

This course is designed to provide you with an understanding of ISO 14971:2019 and the impact it has on the design, development, manufacturing and lifecycle of medical devices. It will also provide medical device manufacturers with knowledge of how ISO 14971:2019 links with the ISO 13485:2016 standard and the MDR 2017/745.

Practical activities throughout the day will give you the opportunity to apply your skills, implementing risk management activities so that these can be embedded within the organization on completion of the course.

"The course has been included in the list of registered public courses under the New Industrialisation and Technology Training Programme."

Each company is subject to a funding ceiling of HK$500,000 in each financial year at the course commencement date.

Please click "here" for the details of NITTP.

How will I benefit?

This course will help you to:

Identify the key requirements of ISO 14971:2019
Interpret and communicate the key requirements and expectations of ISO 14971:2019 to your organization
Gain knowledge of how ISO 14971:2019 links to ISO 13485 and the regulations; MDR 2017/745 and IVDR 2017/746.
Apply the fundamental risk management activities for medical devices within your organization

Who should attend?

This course is ideal for you if you’re in a QA/Regulatory/Engineering/Manufacturing role involved in medical device design, development and manufacturing.

Prerequisites

You should have experience with, or basic knowledge of, quality management systems for the medical device industry. We recommend you have a basic awareness of medical device development, quality assurance and ISO 13485:2016

What will I learn ?

Upon completion of this training, you will be able to:

Define risk management terminology
Explain how risk management relates to the product lifecycle
Outline the stages of the risk management process
Define the key deliverables of the risk management process
Apply risk management principles within your organization
Identify the links between ISO 14971:2019, ISO 13485:2016, MDR 2017/745 and IVDR 2017/746

Our unique accelerated approach fast-tracks learning, improves knowledge retention and ensures you acquire the skills to apply your knowledge straight away. This course involves practical activities, group discussions and classroom learning to help you develop a deeper understanding of the material and have a greater impact on job performance.