How to Configure and Validate GxP Compliant Excel Spreadsheets

How to Configure and Validate GxP Compliant Excel Spreadsheets

Learn how to prevent FDA 483s in 2025 by properly configuring and validating GxP-compliant MS Excel spreadsheet applications.

By Comply Training

Date and time

Wednesday, May 14 · 10 - 11:30am PDT

Location

Online

Refund Policy

Refunds up to 7 days before event

About this event

  • Event lasts 1 hour 30 minutes

This webinar is hosted by TheComplyGuide in partnership with Comply Trainings.

COURSE DESCRIPTION:

This course trains attendees in best practices for creating GxP-compliant spreadsheets using Microsoft Excel. Attendees will learn how to validate applications with minimal documentation.

The instructor will provide step-by-step instructions for configuring Excel to include audit trails, security features, and data-entry verification. Participants will also engage in an interactive workshop to master essential techniques for using Excel spreadsheets for GxP data.

We advise you to bring your laptop to this session and use Excel to gain a complete and guided understanding of developing a GxP-compliant spreadsheet.

During the Q&A, the presenter will address your specific questions, discuss challenging scenarios for each participant, and provide detailed answers.


COURSE OBJECTIVES:

Upon completion of this session, attendees will learn how to:

  • Avoid 483s and Warning Letters
  • Ensure compliance with 21 CFR Part 11 when using Excel spreadsheets for GxP data
  • Use cell and file protections
  • Use Excel’s audit trail
  • Reduce validation time and costs
  • Increase compliance while lowering resource needs
  • Understand what validation documentation is required
  • Address issues and challenges specific to your projects.


AREAS COVERED:

1. Why are spreadsheets so popular?

  • Spreadsheet overview

2. Why is compliance a problem?

  • How is it different from a calculator?

3. Developing Part 11 applications

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

4. Validation

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

5. Using the validated application

  • Maintaining, upgrading, re-validation

6. Examples

  • Requirements
  • Specifications
  • Test cases

7. How to turn on the audit trail

  • How to view the audit trail
  • What are they used for?


COMPLIMENTARY HANDOUTS:

  • User Manual with Excel functions that help to comply with FDA requirements
  • SOP: Validation of spreadsheet applications
  • SOP: Development and use of spreadsheets in regulated environments
  • Gap analysis/checklist for Macros and Spreadsheet applications


WHO WILL BENEFIT:

  • All Excel users in FDA-regulated environments
  • QA Department
  • QC Department
  • IT Department
  • Laboratory staff
  • Managers and Executives
  • Regulatory Affairs
  • Documentation and Validation Specialists


ABOUT THE INSTRUCTOR:

Computer System Validation’s principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, software validation, and computer system validation. He is involved with the development, purchase, installation, operation, and maintenance of computerized systems used in FDA-compliant applications. His most popular book is Risk Based Software Validation - Ten Easy Steps, which provides fill-in-the-blank templates for completing a COTS software validation project.

David has completed more than 300 mission-critical laboratory, clinical, and manufacturing software implementation projects. Services are available to guide companies to create and maintain the systems and procedures required to pass regulatory audits: product features, vendor audits, software validation, SOPs, training, gap analysis, remediation plans, and project management.


Refund Policy:

Attendees may cancel anytime before the webinar, and the refund will be processed within two working days of receiving the cancellation request. Requests for refund should be sent to care@thecomplyguide.com

We will process/provide a full refund if the webinar is canceled. Webinar may be canceled due to lack of enrolment or other unavoidable factors. Attendees will be notified 24 hours in advance if a cancellation occurs.

Participants who register but are unable to attend the webinar will also be provided a refund. On-demand recordings can be requested in exchange too.

Attendees who are not satisfied with the webinar content or quality can request a refund within 24 hours of the completion of the webinar. Refunds will be processed within 48 hours; no questions will be asked.

If you have any questions, please get in touch with us at care@thecomplyguide.com

Organized by

Comply Training is a partner of TheComplyGuide.com

$195 – $695