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SUMMARY:Post-marketing surveillance
DESCRIPTION: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.\nRegister \nWebinar goals\nThe 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: \n\ndefinition of the surveillance system;\nidentification of documentation and key system-related activities;\nobligations of economic operators.\n\nTarget group\nThe webinar is aimed at everyone and is particularly suitable for Quality Assurance/Regulatory Affairs of medical device manufacturers and contract medical device manufacturers. \nWhat we learn from the webinar\nDuring the webinar will be provided notions on the structure of the surveillance system required by the Regulation. \nProgram\n\nDefinitions\nTiming of applicability\nOperators involved\nDocumentation required by the Regulation\n\nLecturer\nIrene 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. \nRegister
URL:https://biopmed.eu/en/evento-en/post-marketing-surveillance/
LOCATION:Online
CATEGORIES:bioPmed events
ATTACH;FMTTYPE=image/jpeg:https://biopmed.eu/wp-content/uploads/2023/03/webinarbioPmed.jpg
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