In the medical device industry, risk management is a vital part of all your company’s processes. Hear from Dr Peter Bowness, Medicinal and Biologics Technical Team Manager, about the updated ISO 14971 and what has changed from the previous version of the standard.
Risk Management for Medical Devices ISO 14971:2019 training course enables a 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.
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.
Upon completion of the Risk Management for Medical Devices ISO 14971:2019 training course, 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 the IVDR 2017/746
Risk Management for Medical Devices ISO 14971:2019 training course is ideal for:
- Managers, Engineers, Executives,
- Supervisors of various departments: Quality Assurance, Production, Regulatory Affairs, Laboratory, Logistics, Purchasing,
- Members of the Risk management Team.
