Computer Software Assurance for Production and Quality System Software

FDA recently issued a guidance document on “Computer Software Assurance for Production and Quality System Software”. This guidance offers clear, practical recommendations for validating software used in medical device production and quality systems. Designed to support compliance with 21 CFR Part 820, this guidance builds on the foundational “General Principles of Software Validation”. It emphasizes […]

Subscribe To AlvaMed's Newsletter

This field is for validation purposes and should be left unchanged.
A monthly analysis of the medical device industry, quality and regulatory developments, and other useful information for industry professionals. (Contact details are never shared outside our organization.)