AAMI TIR57 Medical Device Security Risk Standard Update

A committee draft for vote has been circulated for the AAMI TIR 57 Principles for medical device information security risk management. The objective of this TIR is to provide guidance on how medical device manufacturers can manage risks from security threats that could impact the confidentiality, integrity, and/or availability of the device or the information processed by the device. Because medical device manufacturers are already familiar with ANSI/AAMI/ISO 14971:2007, this guidance follows the basic structure of that standard. AAMI has issued a draft for vote by participating members.

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

Or just email training@softwarecpr.com for more info.

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