From prototype to product, from a CE perspective

About this programme

Contents All companies that sell products on the European market must ensure that their products meet the EU requirements in the EU country where the product is to be sold, to protect human and animal health, the environment and consumer rights. CE marking of a product is required when selling products in the EU. This marking indicate that the product has been assessed by the manufacturer to meet these requirements. The course gives, among other things, an overview of how a company can proceed to meet the requirements set for the development of medical devices. The course provides a overall picture of the basics of CE marking as well as an increased knowledge of product responsibility and product safety. The course also provides an insight into the complex product area medical devices. The course includes compulsory case seminars. The course consists of two modules: 1. Theory 2.5 ECTS 2. Case seminars 1 ECTS Your message goes to Infocenter, and they’ll make sure it gets to the right person – so you get the best and most relevant reply.