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Excel Spreadsheets; develop and validate for 21 CFR Part 11 compliance

Live Webinar | David Nettleton | Jul 30, 2026 , 01 : 00 PM ET | 90 Minutes |  2 Days Left

Description


This interactive webinar explains how to configure and validate GxP-compliant spreadsheet applications 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.

What you'll learn?

Why are spreadsheets so popular

  • Spreadsheet overview
  • What are they used for

Why is compliance a problem

  • How is it different from a calculator

Developing Part 11 applications

  • Security
  • Versioning
  • Cell protection
  • Data entry checks
  • Audit trail
  • Data output formatting

Validation

  • Fill-in-the-blank validation templates
  • Step-by-step validation

Using the validated application

  • Maintaining, upgrading, re-validation

Examples

  • Requirements
  • Specifications
  • Test cases

How to turn on the audit trail

  • How to view the audit trail

    Why should you attend?

    Attend this webinar to:

    • Learn how to use Excel’s built-in 21 CFR Part 11 features
    • Develop spreadsheet applications that are GxP compliant
    • 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 Professionals
    • QA
    • QC
    • Laboratory staff
    • Managers and Directors
    • Executives
    • Auditors
    • GMP, GCP, GLP, Regulatory Professionals

    Training Price

    Live Session     $179
    Recording     $199
    Digital Download     $229
    Transcript (PDF)     $199
    Corporate Live 1-10-Attendees     $999
    Live+Recording     $349
    Recording+Transcript     $349
    Digital Download+Transcript     $399



    Over 10 Attendees Registration ?


    Any Organization, Institution or Group User can register

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