21 CFR Part 11 for Particle QC Applications

Overview

This webinar provides an essential overview of implementing and optimizing digital records processes for 21 CFR Part 11 compliance specifically for pharmaceutical Quality Control environments. We cover the historical shift from manual to digital QC data, and how to assess your digital records process for compliance with quality guidelines. Gain important insights into navigating compliance challenges, ensuring audit readiness, and achieving a successful 21 CFR Part 11 implementation for particle analysis data.