How medical device manufacturers realize, apply and document risk management according to ISO 14971 / EN ISO 14971.
All medical device manufacturers must implement and document a risk management process. Learn how to implement the requirements of ISO 14971:2019 / EN ISO 14971 over all life cycles for your medical device and take into account the changes of the third edition from 2019. You will learn how to perform a risk analysis, correctly assess the risks and successfully minimize them.
Nutzen
You will get an overview of the current regulatory requirements for risk minimization that manufacturers of medical devices must comply with.
You will learn about the contents and requirements of ISO 14971:2019 / EN ISO 14971 as well as the purpose and procedure of a risk analysis.
You will be enabled to systematically implement the risk management process in your company.
You will deepen your knowledge with practical examples.
Abschluss
Teilnahmebescheinigung
Certificate of attendance
Zielgruppe
The seminar is for regulatory affairs specialists, quality management specialists as well as employees from the areas of quality and product management, design and development from companies in the medical device industry.
Inhalte
Regulatory requirements to minimize the risks associated with medical devices
Requirements of European regulations (MDR, IvDR)
Risk management EN ISO 14971 vs. quality management EN ISO 13485 - Risk-based approach to products and QMS processes
ISO 14971:2007 vs. ISO 14971:2019
new and amended terms and definitions
Structure and set-up
Risks, hazards and their evaluation
Procedure and methods for risk analysis (e.g. fault tree analysis, FMEA)
Risk management versus risk analysis
Holistic risk assessment over the entire life cycle and connection with post market surveillance
Documentation in risk management
Hinweise
The seminar contents take into account the current status of regulations/harmonization
