Courses
Navigating FDA cGMP Regulations: Mastering 21 CFR 210, 211, and 820
Crack the Code of 21 CFR 820 and FDA Inspections!
John E Lincoln
Evolving Audit Trails: Mastering Data Integrity and FDA 21 CFR Part 11 Compliance
Empower Your Compliance Journey: From Basics to Best Practices!
Carolyn Troiano
Mastering FDA Audits: A 6-Hour Virtual Seminar on Preparing, Conducting, and Executing with Confidence
Are You Prepared for the Toughest Scrutiny FDA Inspectors Can Bring to Your Door?
Charles H. Paul
Managing Toxic & Other Employees Who Have Attitude Issues
Effective Approaches for Addressing & Preventing Toxicity – Organization-wide!
Pete Tosh
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
Engaging Employees in 2024: Key Drivers of Employee Engagement
Learn Proven Principles and Practices for a Wold-Class Employee Engagement.
Don Phin
Risk Management for Medical Devices: Complying with ISO 14971:2019 and FDA Latest Requirements
Ensure Your ISO 14971 Compliance Evolves With Your Device Innovations And Unseen Risks Of Tomorrow’s Technologies!
Jose Mora
Mastering Compliance for FDA-Regulated Systems: Leveraging CSA and GAMP®5 Second Edition
Struggling to Balance Innovation with Compliance in FDA-Regulated Systems?
Carolyn Troiano
Master Risk-Based Design Control: The Key to Compliant and Innovative Medical Device Design
Innovate with Confidence: Risk-Based Design Control for Cutting-Edge Medical Devices!
Jose Mora
Human Error No More: Supervision Tactics to Build an Error-Free Workplace
Master Supervisory Strategies to Reduce Mistakes and Enhance Team Productivity!
