Excel Spreadsheet Validation for Part 11 to Eliminate 483s
David Nettleton
January 26,2026
1:00 PM EST
75 Minutes
Live Webinar
Pharmaceutical
5 Days Left
This interactive webinar explains how to configure and validate a GxP-compliant spreadsheet application to avoid FDA 483s. Follow the step-by-step instructions as we configure Excel for audit trails, security features, and data entry verification. Understand how to validate your application with minimal documentation. Bring your laptop and use Excel for your own needs. This session will make you a better Excel user, saving you time and costs.
Areas Covered:-
- Develop spreadsheet applications that are GxP compliant
- Learn how to use Excel’s built-in 21 CFR Part 11 features
- Apply features required for GxP environments without programming macros.
- Follow along as we configure Excel for audit trails, security features, data verification, and multiple concurrent users
- Avoid 483s and Warning Letters
- How to use cell and file protections
- Reduce validation time and costs
- Increase compliance while lowering resource needs
- Validate your application with minimal documentation
- Understand what does and does not need to be validated.
- How to specify and test your application.
Who Should Attend?
- All Excel users
- IT
- QA
- QC
- Laboratory staff
- Managers
- Executives
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Computer System Validation’s principal, David Nettleton, is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, EU General Data Protection Regulation (GDPR), software validation, and computer system validation. He is involved with developing, purchasing, installing, operating, and maintaining computerized systems used in FDA-compliant applications. He has completed more than 300 mission-critical laboratory, clinical, and manufacturing software implementation projects. His most recent book is Software as a Service (SaaS) Risk-Based Validation With Time-Saving Templates, which provides fill-in-the-blank templates for completing a COTS software validation project.
