FDA added a number of new online training modules for medicla device compliance to its CDRHLearn curriculm at the link provided. Some of the new modules foucs on Benefit-Risk evaluation, Global Harmonization, Labeling, and In vitro diagnostics
IEC 62304 and other Emerging Standards Impacting Medical Device Software
Being Agile & Yet Compliant
ISO 14971 SaMD Risk Management
Software Risk Management
Medical Device Cybersecurity
Software Verification
IEC 62366 Usability Process and Documentation
Or just email training@softwarecpr.com for more info.