GxP Computer System User Requirements Generator

This agent transforms days of requirements writing into minutes by generating complete, GxP-compliant User Requirements Specifications (URS) with fully numbered, traceable requirements. Built by a 25-year pharmaceutical validation expert using current FDA CSA Guidance (February 2026), GAMP5 2nd Edition, and 21 CFR Part 11 requirements, it delivers audit-ready URS documentation for LIMS, QMS, MES, CDS, ELN, LMS, and custom GxP systems. Every requirement is written in SHALL language with testable acceptance criteria and verification method assignments — ready to drive FRS authoring, risk assessment, and IQ/OQ/PQ protocol development. Perfect for validation leads, QA engineers, pharmaceutical quality managers, biotech compliance teams, and medical device quality professionals who need a traceable, inspection-ready URS without starting from a blank page.