21 CFR Part 11 for Particle QC Applications

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 will 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.

Webinar Objectives

• Understand the critical elements an auditor looks for when evaluating 21 CFR Part 11 compliance in a QC lab
• Identify which 21 CFR Part 11 regulations are tied to these critical compliance elements
• Learn strategies for assessing and improving digital record processes to ensure compliance and prepare for audits

Secure your spot today and take the first step toward seamless 21 CFR Part 11 compliance.

2025-GBL-EN-108211-v1