This white paper provides an update of the proposed revisions to EU medical device regulation as of April 2014. BSI WP EU Regulations
This white paper provides an update of the proposed revisions to EU medical device regulation as of April 2014. BSI WP EU Regulations
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.