6. MDR ADVERSE EVENT REPORTING IN CLINICAL INVESTIGATIONS
Clinical Trials for Medical Devices in EuropeDuration:  Unlimited
Cost:  179  USD
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.
![](https://academy.mastertrial.com/pluginfile.php/3284/course/overviewfiles/EU%20102-F%20MDR%20Clin.%20Inv.%20Adverse%20events%20reporting%20Rev.10%2003Aug2020.jpg)
Length: 00:15