Product development of biomedical devices
In addition to various studies and plans, a schedule and budget are made for the project and the cost structure of the product is determined. At the end of the course, the product and project are presented to a jury which evaluates them.
Join this course to deepen your skills!
This course is part of Health technology solutions – product development and commerzialization study module. Get acquainted with the study module and other courses included in it. The study module offers a formal additional education for a “Person responsible for regulatory compliance” required by the new EU regulations in Medical Devices Regulation (MDR) and In-vitro Diagnostics Regulation (IVDR).