The compartment of Medical Devices: how it is constituted and which are the main regulatory requirements
Dr. Fabrizio Cannioto, Research Centre Analyst
Dr. Fabio Cubeddu, Quality & Regulatory Affairs Specialist, Confindustria-Dispositivi Medici (Milano)
DEIB - Conference Room (Building 20)
July 25th, 2022
4.30 pm
Contacts:
Sergio Cerutti
Dr. Fabio Cubeddu, Quality & Regulatory Affairs Specialist, Confindustria-Dispositivi Medici (Milano)
DEIB - Conference Room (Building 20)
July 25th, 2022
4.30 pm
Contacts:
Sergio Cerutti
Abstract
On July 25th, 2022 at 4.30 pm Dr. Fabrizio Cannioto, Research Centre Analyst, Dr. Fabio Cubeddu, Quality & Regulatory Affairs Specialist, Confindustria-Dispositivi Medici (Milano) will held a seminar on “The compartment of Medical Devices: how it is constituted and which are the main regulatory requirements”, in DEIB Conference Room (building 20, via Ponzio 34/5, Milano).
The seminar can be followed remotely via Webex (password RVdYkzSb473).
The seminar is organised on occasion of the visit at the Politecnico di Milano from a delegation of Students in Biomedical Engineering from the University of Delft (The Netherlands), in cooperation with Confindustria-Dispositivi Medici, on the Regulatory Aspects of Medical Devices.
The Seminar was mainly designed for Post-Docs, Master and PhD Students, but it is open to a wider audience.
The seminar can be followed remotely via Webex (password RVdYkzSb473).
The seminar is organised on occasion of the visit at the Politecnico di Milano from a delegation of Students in Biomedical Engineering from the University of Delft (The Netherlands), in cooperation with Confindustria-Dispositivi Medici, on the Regulatory Aspects of Medical Devices.
The Seminar was mainly designed for Post-Docs, Master and PhD Students, but it is open to a wider audience.
