Upcoming webinars
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
Computer System Validation (CSV) vs. Computer System Assurance (CSA): Applying an Agile Methodology vs. Waterfall for FDA-Regulated Computer System
Master A Risk-based, Product Quality, and Patient-Centric Approach to Computer System Assurance (CSA)!
Carolyn Troiano
Stay Ahead of the Curve: Analytical Method Validation Under Good Laboratory Practices (GLPs)
Don’t Leave Accuracy to Chance: Master Analytical Method Validation in GLP!
John Fetzer
Cybersecurity Compliance For Medical Devices: Align With Latest FDA Standards
Protect Patient Data and Ensure Compliance in a Rapidly Evolving Landscape!
John E Lincoln
Quality Management 101: Optimizing Enterprise Maintenance with ISO Standards
Transform Maintenance With ISO 9001 Insights for Proactive, Quality-Driven Results!
John E Lincoln
Data Integrity in GMP and GCP: Compliance with FDA, EMA, and MHRA Requirements
Ensure Global Compliance With Bulletproof Data Integrity Practices!
Charles H. Paul
6-Hour Virtual Seminar on Inspection and Audit Readiness Training for Medical Device Manufacturers
Safeguard Compliance And Minimize Risk With Proven Best Practices!
John E Lincoln
2025 FDA & ISO Process Validation Mastery: Advanced Process Validation for Global Regulatory Alignment
Stay Ahead or Pay the Price – Learn Cutting-Edge Strategies to Prevent Costly Compliance Mistakes!
Jose Mora
Beyond Compliance: Perfecting 21 CFR Part 11 for FDA-Regulated Computer Systems
Future-Proof Your Compliance: Adapting to 21 CFR Part 11 in 2024!
Carolyn Troiano
Data Integrity & FDA Governance: Modern Strategies for Regulated Computer Systems
Empower Your Compliance: Proactive Strategies for System Integrity & Compliance!
