Graham O'Keeffe

Why Changes to Equipment and Documentation Play a Vital Role in GMP

Potential Areas Of Use For Risk Management Tools

Choosing the Best Regulated Software for Your Organization – My Top 5 Tips

Top 9 Tips for Successful Implementation of FMEA

How to Create a Bullet-Proof User Requirement Specification (URS)

Best Practice – Creating a Typical Validation Test Protocol (With Video Demo)

9 Things to Consider with CSV Periodic Reviews

21 CFR Part 11 A Dummies Guide Part 3 – Sec. 11.3 Definitions

Approval Cycles for Validation Documents – Overview

How to Deploy a Software Application in a GxP Environment – Planning and Design