The slides from a presentation on AAMI/IEC 62304 by FDA’s Device Center Software Compliance expert (John Murray) are at the link provided. These were presented at a trainng course Sept 15-17 on medical device software standards.
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.