This seminar provides a detailed introduction to the European medical device legislation. It will explain the regulation and which products are covered, the involvement of Notified Bodies, and how to choose one. It will also outline what a manufacturer must do.
An Introduction to the Medical Device Regulation
Nov 10th, 2019Nov 12th, 2019
London, 17
GB
Phone:2077494730
Latest in Home
Smart Reporting secures €23M in financing
April 25, 2024
First patient dosed with ITM-31 in glioblastoma trial
April 23, 2024
ESR releases movie to mark key moments of ECR 2024
April 23, 2024