3. MDR CONDITIONS, ETHICAL PRINCIPLES, METHODS, INFORMED CONSENTClinical Trials for Medical Devices in Europe
Cost:  179  USD
This lecture investigates the new Medical Device Regulation (MDR) with regard to conditions, ethical principles, methods and informed consent process. The intent of this tutorial is to describe the conditions for carrying out clinical investigations and to outline the rules laid down by MDR for particular clinical investigation types.