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Post-marketing surveillance
March 28, 2023 @ 11:30 AM - 12:30 PM
A webinar that offers an overview of post-market surveillance in accordance with the Medical Devices Regulation 2017/745 with ad hoc notions on the structure of the surveillance system.
Webinar goals
The webinar will provide an overview of post-market surveillance in accordance with the Medical Devices Regulation 2017/745. The meeting will address issues such as:
- definition of the surveillance system;
- identification of documentation and key system-related activities;
- obligations of economic operators.
Target group
The webinar is aimed at everyone and is particularly suitable for Quality Assurance/Regulatory Affairs of medical device manufacturers and contract medical device manufacturers.
What we learn from the webinar
During the webinar will be provided notions on the structure of the surveillance system required by the Regulation.
Program
- Definitions
- Timing of applicability
- Operators involved
- Documentation required by the Regulation
Lecturer
Irene Giovanetto. Biomedical engineer, with a degree from the Polytechnic of Turin. Since 2019 he has been collaborating with Chemsafe S.r.l. for regulatory advice on medical devices.
