Upcoming webinars

The Danger of AI

FDA-Compliant Validation Of AI, ML, And Super-intelligent Systems

Unlock the Potential of AI with Compliance Confidence!

Carolyn Troiano

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

APR 22, 2025 (TUE)

FDA Compliance

How to Comply with the FDA’s Quality System Regulation (QSR) – 21 CFR Part 820

Build Your Thorough Understanding of The Regulation to Ensure You are Compliant to It.

Charles H. Paul

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

APR 22, 2025 (TUE)

What is Required for 21 CFR Part 11 Compliance?

21 CFR Part 11 Compliance for Computer Systems Regulated by FDA: Compliance Chaos or Crystal Clarity? A 6-Hour Deep Dive

Avoid FDA Enforcement Action: Unlock the 2024 Roadmap to Compliance Before It’s Too Late!

Carolyn Troiano

6 Hrs.| 08 AM PT - 02 PM PT | USD 759

APR 22, 2025 (TUE)

MEDIATION SKILLS FOR LEADERS

Why Aren’t Your Team Members Speaking Up – Mediation Skills To Turn Resistance into Cooperation

Avoid The Drawbacks of Traditional Conflict Resolution & Create Lasting Solutions!

Ben Adkins

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

APR 22, 2025 (TUE)

Excuse Makers handling

Difficult Employees Sabotage and Obstruct Work Projects: How to Transform Excuse Makers into Accountable Leaders

Strategies for Dealing with Different Types of Difficult Employees at Work!

Bob Churilla

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

APR 22, 2025 (TUE)

CAPA

How FDA trains its Investigators to Review CAPA and How should you prepare

Learn Step-By-Step Methods to Initiate, Manage, And Close CAPAs Effectively to Ensure Compliance!

Charles H. Paul

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

APR 22, 2025 (TUE)

Computer System Validation

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

90 Mins.| 10 am PT | USD 189

APR 22, 2025 (TUE)

Analytical Method Validation

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

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

APR 22, 2025 (TUE)

MEDICAL DEVICE CYBERSECURITY FDA COMPLIANCE

6-Hour Virtual Bootcamp on Medical Device Cybersecurity: Shield Your Data, Ensure FDA Compliance, Lead with Confidence

Implement Advanced Risk Management, Develop A Robust SQA Plan, & Stay Ahead of Emerging Cybersecurity Threats!

Carolyn Troiano

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

APR 23, 2025 (WED)

FDA 510 k Submission Process

Navigating FDA 510(k) Submissions: How to Sidestep Common Mistakes and Ensure Approval

Learn From the Pros to Get it Right the First Time and Get Your Product to Market Faster!

Charles H. Paul

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

APR 23, 2025 (WED)

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