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:
- Interpret the regulations pertaining to Risk Management and ISO 14971 in particular.
• Identify and quantify risks associated with medical devices.
• Decide on the acceptability of those risks.
• Re-evaluate risks following corrective action.
• Different advanced risk assessment techniques.
• HAZOP methodology and its applications.
• Quantitative Risk assessment (QRA).
• 3 types of evaluation of risks: Qualitative, Semi-Quantitative and Quantified.
• Methodology of Failure Mode and Effects analysis (FMEA).
• Evaluating risk control, residual risk and acceptable risk, in term of the safety of medical devices
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.
