Courses
From Boring Data to Brilliant Stories: Master Excel Like a Pro
What If You Could Transform Your Data Into Compelling Stories That Inspire and Persuade?
Terry Winship
4-Hours Virtual Seminar on GxP/GMP and Its Consequences for QA, Change Management, Documentation and IT Systems
Manage and Control Documents in Compliance with GxP/GMP Requirements and Pass Any Quality Audit.
Eleonora Babayants
FDA Technology Modernization Action Plan (TMAP) and Impact on Regulated Computer Systems and Data Integrity
Ensure System Compliance Amid FDA’s Rapid Technology Transformation!
Carolyn Troiano
Project Management for Computer System Validation (CSV) to Improve FDA Compliance
Enhance CSV Projects: Embrace Project Management!
Carolyn Troiano
Mastering the Human Error Toolbox: How to Predict, Prevent, and Overcome Costly Mistakes
Discover the Psychology Behind Human Error and What Drives Critical Mistakes!
Ginette Collazo
Master Project Management: A 6-Hour Virtual Workshop for Non-Project Managers
Learn, Lead, and Excel—Manage Projects with Confidence and Clarity!
Charles H. Paul
2-Hour Virtual Masterclass: Avoiding FDA Software Validation Nightmares – The Top 6 Compliance Failures and How to Tackle Them in 2025
What if Your Software Validation is Setting You Up for An FDA Failure?
David Nettelton
Onboarding 2025: Blending Virtual & In-Person Onboarding to Welcome, Engage & Retain New Hires
A Poorly Designed Onboarding Process Can Result in A New Hire’s Emotional Exhaustion & Job Burnout!
Diane Dee
SOPs – How to Write Them to Satisfy Those Inspectors
Are Your SOPs A Ticking Compliance Time Bomb in The Eyes of The FDA?
Meredith Crabtree
Stay Compliant with FDA’s New Draft on Software & Device Modifications: A 510(k) Update
Are You Certain Your Next Software or Device Update Won’t Require A New 510(k)?
