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This course presents an overview of the "actors" within the scope of the new MDR, namely the sponsors, investigators, and subjects. Learn all you need to know about how these "actors" play a significant role within the new MDR. After the course, you can take a brief test to receive your certification. Enjoy!
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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.
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This tutorial aims to provide an overview of the MDR provisions related to the end of the clinical investigation, along with an outline of the MDR rules concerning the extraordinary events which could happen during the clinical investigation (substantial modifications, corrective measures, temporary halt, early termination).
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The purpose of this tutorial is to analyze the MDR provisions for adverse events recording and reporting to Competent Authorities. The topics addressed are: MDR references, Relevant definitions, Sponsor obligations in case of adverse events occurring during the clinical investigation and Regulatory comparison: MDD vs MDR.
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Get Certified Today!
Do you need an MPG certificate to carry out clinical trials with medical devices? Would you like to deepen your knowledge? This Mastertrial MPG/GCP course is all online and is recognized by the Berlin Medical Association (CME). This Basic Course offers the following accredited training course for principal examiners, examiners and members of the examination group. Download the MPG courses brochure
Clinical Trials in Europe and the US
Stay up to date with the latest in MPG requirements