Congressional hearing on SW as a Device

The link provided is to an article on mobihealthnews.com summarizing the congressional hearing last week on whether software should be regulated by FDA as a medical device. This is related to the Blackburn Bill which would exempt many standalone software medical applications, if passed into law, from FDA regulation.

SoftwareCPR Training Courses

IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software

ISO 14971 Risk Management (typically with heavy emphasis on software aspect)

IEC 81001-5-1 Cybersecurity Lifecycle

ISO 13485 QMS Requirements & optionally ISO 19011 for leading audits

Being Agile Yet Compliant (AAMI TIR 45)

IEC 29119-1 Software and System Testing

US Classification for Software Devices

IEC 62366 Usability Process and Documentation

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