CoRE training – Spring 2019, Los Angeles, CA Click a title to view recording Definitions & Classifications, Part 1 Definitions & Classifications, Part 2 Risk Management Design Controls and Active Medical Devices Environmental and Human Factors In Vitro Diagnostic Devices Infection and Microbial Contamination Role of Standards Essentials of Conformity Assessment Risk Analysis workshop Medical Devices 101: Labeling and UDI Audits and the MSDAP Program (PowerPoint slides)Download Agenda from original trainingDownload