Spreadsheets are everywhere in GxP work, and poorly controlled ones lead to FDA 483s. This interactive 75-minute webinar shows how to develop and validate Excel spreadsheets for 21 CFR Part 11 compliance, step by step.
You'll follow along as Excel is configured for audit trails, security, versioning, cell protection, data entry checks, output formatting and multiple concurrent users, using Excel's built-in Part 11 features rather than macros. Bring your laptop and work on your own spreadsheets.
The session then covers validation with fill-in-the-blank templates and minimal documentation, what does and doesn't need validating, and how to maintain, upgrade and revalidate the application.
WHY SHOULD YOU ATTEND?
Spreadsheets are hard to keep compliant, and gaps can lead to 483s and Warning Letters. This session shows how to build GxP-compliant spreadsheet applications, raise compliance while using fewer resources, and cut validation time and cost.
It suits all Excel users, IT, QA, QC, laboratory staff, managers, executives, auditors, and GMP, GCP, GLP and regulatory professionals.
AREA COVERED
1. Why spreadsheets are so popular
- Spreadsheet overview
- What spreadsheets are used for
2. Why compliance is a problem
- How a spreadsheet differs from a calculator
3. Developing Part 11 applications
- Security
- Versioning
- Cell and file protection
- Data entry checks
- Audit trail
- Data output formatting
- Multiple concurrent users
4. Validation
- Fill-in-the-blank validation templates
- Step-by-step validation
- What does and does not need to be validated
5. Using the validated application
- Maintaining, upgrading and revalidating
6. Examples
- Requirements
- Specifications
- Test cases
7. Audit trail in practice
- How to turn on the audit trail
- How to view the audit trail
LEARNING OBJECTIVES
- Develop GxP-compliant spreadsheet applications in Excel
- Use Excel's built-in 21 CFR Part 11 features without programming macros
- Configure audit trails, security, data verification and cell and file protection
- Specify and test a spreadsheet application
- Validate the application with minimal documentation
- Decide what does and does not need to be validated
WHO WILL BENEFIT?
- All Excel users.
- IT.
- QA.
- QC.
- Laboratory staff.
- Managers.
- Executives.
- Auditors.
- GMP, GCP, GLP, regulatory professionals.
Spreadsheets are hard to keep compliant, and gaps can lead to 483s and Warning Letters. This session shows how to build GxP-compliant spreadsheet applications, raise compliance while using fewer resources, and cut validation time and cost.
It suits all Excel users, IT, QA, QC, laboratory staff, managers, executives, auditors, and GMP, GCP, GLP and regulatory professionals.
1. Why spreadsheets are so popular
- Spreadsheet overview
- What spreadsheets are used for
2. Why compliance is a problem
- How a spreadsheet differs from a calculator
3. Developing Part 11 applications
- Security
- Versioning
- Cell and file protection
- Data entry checks
- Audit trail
- Data output formatting
- Multiple concurrent users
4. Validation
- Fill-in-the-blank validation templates
- Step-by-step validation
- What does and does not need to be validated
5. Using the validated application
- Maintaining, upgrading and revalidating
6. Examples
- Requirements
- Specifications
- Test cases
7. Audit trail in practice
- How to turn on the audit trail
- How to view the audit trail
- Develop GxP-compliant spreadsheet applications in Excel
- Use Excel's built-in 21 CFR Part 11 features without programming macros
- Configure audit trails, security, data verification and cell and file protection
- Specify and test a spreadsheet application
- Validate the application with minimal documentation
- Decide what does and does not need to be validated
- All Excel users.
- IT.
- QA.
- QC.
- Laboratory staff.
- Managers.
- Executives.
- Auditors.
- GMP, GCP, GLP, regulatory professionals.
Speaker Profile
David Nettleton
Computer System Validation’s principal, David Nettleton is an industry leader, author, and teacher for 21 CFR Part 11, Annex 11, HIPAA, EU GDPR 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. 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.
Upcoming Webinars
New Form I-9: Documents and Policies that Ensure ICE I-9 Co…
Claude AI For CPAs & Finance Professionals: Best Practices …
Secrets Of Psychology - Why People Do The Things They Do
2-Hour Virtual Seminar on How to Conduct an Internal Harass…
Project Management For Administrative Professionals
Elevate Your Workplace Wellness: 10 Critical Wellness Facto…
Onboarding is NOT Orientation - How to Improve the New Empl…
Managing Complex Projects - Project Management
Utilizing HR Metrics to Illustrate & Improve Human Resource…
Negotiating Skills For Professional Results - Winning Strat…
NEW Nacha Rule - Third-Party Sender (TPS) Roles and Respons…
FDA Technology Modernization Action Plan (TMAP) and Impact …
Paying and Receiving Payments for Referrals: You Can Go to …
Validation Statistics for Non-Statisticians
Human Factors Usability Studies Following ISO 62366 and FDA…
Construction Lending And Real Credit Administration: Evalua…
Excel Power Skills: Master Functions, Formulas, and Macros …
Thriving in a Hybrid Workplace: Keys to Leadership and Team…
Batch Record Review and Product Release
Discover how Emotional Intelligence turns AI from a technic…
Female to Female Hostility @Workplace: All you Need to Know
Copilot and HR: An Introduction for HR Professionals
ChatGPT for HR - Build HR Policy Framework and Strategy
Excel Spreadsheets; Develop and Validate for 21 CFR Part 11…
The Perfect Storm Coming to Healthcare: Value Based Care Me…
Language is Code - Intro to AI - Generative AI - ChatGPT an…
Major cGMP Issues: FDA Concerns in 2026
I-9 Audits: Strengthening Your Immigration Compliance Strat…
Pivot tables beginner to advanced + 20 advanced Pivot table…
Emotional Intelligence: Mastering the Emotions of Great Lea…