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
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Documentation Files – The US FDA and EU MDR Requirements
Ensure Global Compliance With Expert Insights On Key Documentation!
John E Lincoln
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
Mastering Verification & Validation: Building a Compliant V&V Plan Aligned With FDA, ISO 13485 & ISO 14971
Ensure Regulatory Compliance With A Robust, Audit-Ready V&V Strategy!
John E Lincoln
FDA-Compliant Validation Of AI, ML, And Super-intelligent Systems
Unlock the Potential of AI with Compliance Confidence!
Carolyn Troiano
Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements
Ensure Global Compliance With Bulletproof Data Integrity Practices!
