IEC/TR 62348 Assessment

IEC/TR 62348 is a technical report that assesses “the impact of the most significant changes in Amendment 1 to IEC 60601-1:2005 and mapping of the clauses of IEC 60601-1:2005 to the previous edition.”  The report is intended to be a tool for manufacturers to understand the impact of Amendment 1:2012 changes to 60601-1 from the 2005 version.

From a software perspective, the report indicates “moderate impact” related to section 14 Programmable Electrical Medical Systems or PEMS.  The 2005 update to IEC 60601-1 specified that a “development process” is required for all Programmable Electronic Subsystems (PESS) including software.  That update included informative references to IEC 62304 for information on software since 62304 was soon to be released at that time.  For manufacturers that incorporated full IEC 62304 compliance into their development process, amendment 1 creates no additional requirements.  If a development process was put into place but it was not fully compliant with IEC 62304, conformance with amendment 1 will require full compliance with IEC 62304.

We would further remind our clients of the specific requirements for software risk analysis required by 62304 as this may not have been explicit in the existing risk management policies and procedures.

About the author

Partner and General Manager, Brian Pate is ISO 1385:2016 Lead Auditor certified for Medical Device Quality Management Systems (MD), and ISO 19011:2018 Management Systems Auditing (AU) and Leading Management Systems Audit Teams (TL). Brian started his medical device career in anesthesia clinical research in 1985 and has since worked both academia and industry including many years with Johnson & Johnson, Baxter Healthcare, and GE Medical. Brian’s roles have included software engineering, systems engineering, quality assurance, and regulatory affairs. Brian has served on multiple AAMI TIR working groups, including TIR32-2008 (Application of ISO 14971 Risk Management to Software; now IEC 80002-1) and TIR45-2012 (Guidance on the use of Agile practices in the development of medical device software) and served as a reviewer for the 2nd edition of TIR45. Brian serves on the AAMI Software Committee and as an AAMI instructor for the software, design controls, and agile methods courses. Brian also is a member of the Underwriters’ Laboratories (UL) Standards Technical Panel for UL1998 (Software in Programmable Components) and or UL5500 (Remote Software Updates).

SoftwareCPR Training Courses

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

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