- TypeWebinar
- Location Los Angeles, California, United States
- Date 19-11-2020
Administration/Management
Information Technology
Biotechnology
Manufacturing
Medical/Healthcare/Hospital
This course will give an introduction into the new ISO 14971:2019 and how to create a risk management file according the ISO 14971:2019. It will give you an overview about the requirements the interfaces to Post-Market-Surveillance, Clinical Evaluation, Bench-Testing and Life-Cycle-Management. and how a smart implementation of these requirements in your product documentation is possible and finally what are the expectations of the European Notified Bodies.