Courses

Implementing Impactful CAPA

Implementing Impactful CAPA: Root Cause Analysis & Effectiveness Checks

Are Your Corrective Actions Making A Difference, Or Just Ticking Boxes?

Meredith Crabtree

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

JAN 06, 2025 (MON)

Quality Management and Quality Audit

Quality Management and Quality Audit According to Gxp/GMP Requirements

Complete Guide to Learn GxP/GMP Regulations How They Affect Quality Management System and Quality Audit. Get Audit Ready Today!

Eleonora Babayants

90 Mins| 10 AM PT - 11:30 AM PT | USD 229

JAN 06, 2025 (MON)

Courageous Conversational Skills

Silent But Unhappy Team Members – Create an Insanely Positive and Productive Workplace Culture

Are Hidden Tensions Stifling Your Team’s Potential & Innovation?

Larry Johnson

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

JAN 07, 2025 (TUE)

Navigating FDA cGMP Regulations

Navigating FDA cGMP Regulations: Mastering 21 CFR 210, 211, and 820

Crack the Code of 21 CFR 820 and FDA Inspections!

John E Lincoln

1 Hr.| 10 AM PT - 11 AM PT | USD 229

JAN 07, 2025 (TUE)

Evolving audit trials

Evolving Audit Trails: Mastering Data Integrity and FDA 21 CFR Part 11 Compliance

Empower Your Compliance Journey: From Basics to Best Practices!

Carolyn Troiano

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

JAN 07, 2025 (TUE)

Mastering FDA Audit

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

6 Hrs.| 9 AM PT - 3 PM PT | USD 759

JAN 07, 2025 (TUE)

How-to-Manage-Toxic-Employees

Managing Toxic & Other Employees Who Have Attitude Issues

Effective Approaches for Addressing & Preventing Toxicity – Organization-wide!

Pete Tosh

1 Hr.| 10 AM PT - 11 AM PT | USD 209

JAN 07, 2025 (TUE)

SOPs

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

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

JAN 07, 2025 (TUE)

Leveraging CSA and GAMP®5

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

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

JAN 08, 2025 (WED)

Design Control Basics

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

90 Mins.| 9 AM PT - 10:30 AM PT | USD 229

JAN 08, 2025 (WED)

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