FDA CSA Guidance

After many years of navigating the difficult task of properly validating quality system and production software tools, FDA released the “Computer Software Assurance for
Production and Quality Management System Software Guidance for Industry and Food and Drug Administration Staff” on February 3, 2026. While this release may have not been noticed by many, it is very significant, in our opinion, because it solidifies the FDA intent to expect (and accept) risk based approaches to validating these tools rather than a “one size fits all” inefficient and rote approach. The manufacturer is encouraged to analyze the most effective approach, holistically across all software tools.

You can download the guidance here:  2026-guidance-computer-software-assurance-production-quality-system

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).

Upcoming Public Courses

IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software training course in Boise, Idaho. 3-Day course.

October 13-15, 2026

Limited Early Bird Registration: $995 / person
Non refundable but transferable.

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

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