FDA issued a Draft guidance “Complementary and Alternative Medicine Products and Their Regulation by the Food and Drug Administratione” dated December 2006..Sections of this guidance discuss cogninitve/behavioral functionality. This may be helpful for software products that are for personal behavioral use.
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.
