AI is transforming pharmaceutical microbiology, freeing teams from manual plate reading and accelerating turnaround times. But implementing intelligent automation isn’t just about speed. It must be able to perform in the real-world lab environment and stand up to GxP requirements.
In this whitepaper, explore how a pharma microbiology program can confidently adopt AI-enabled automated plate reading systems while staying compliant in GxP environments. It provides a practical, risk-based approach to validation that shifts the focus from “black box” concerns to system performance, intended use, and data integrity.
Covering the full lifecycle from selection and qualification to ongoing monitoring and change management, our subject matter experts provide clear guidance on meeting regulatory expectations while unlocking the efficiency and consistency benefits of automation in pharmaceutical manufacturing.
This is a must-read for organizations looking to modernize microbiology operations without compromising compliance.
