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3. MDR CONDITIONS, ETHICAL PRINCIPLES, METHODS, INFORMED CONSENT
Clinical Trials for Medical Devices in EuropeDuration: Unlimited
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.
Length: 00:20