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
ISO13485:2016 ISO 13485 Internal Audit(or) Training Course (Live, 3-day)
IEC 62304 and other Emerging Standards Impacting Medical Device Software (Live, 3-day)
Being Agile & Yet CompliantISO 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.