Cleaning Validation Direct-to-Site Live Mini Workshop

🧼 What FDA Expects in a Cleaning Validation Report

A Mini-Workshop for QA, Validation, and Regulatory Professionals
Hosted by: DeVaughn Edwards, Former FDA Investigator & Principal Consultant, FDAID, LLC

🎯 What You’ll Get:

This 30-minute live Zoom workshop dives into what the FDA actually expects when reviewing your cleaning validation reports. No fluff. No generic training slides. Just the key points you need to stay inspection-ready—in less time than your lunch break.

🧪 What We’ll Cover:

• Core report components: protocol, limits, sampling methods, and conclusion
• Swab vs. rinse: how to choose, justify, and defend
• MACO, NOEL, PDE, and why 10 ppm is NOT a free pass
• Data integrity and audit trail expectations
• Common FDA findings—and how to avoid them
• Real case study based on an FDA Warning Letter

✅ Why This Training Is Different:

• Built by former FDA Investigators—not AI or copy-paste
• Designed for real-time use in your job, not theoretical nonsense
• Live and human-led (because you’re not getting inspected by a bot)
  

Includes live Zoom access

• Quiz (optional and may be taken at any time after the session ends)
• Certificate of completion (for those that complete and pass the quiz)
• PowerPoint slides available for purchase
• Optional: Add the full PowerPoint slide deck for an additional $10. Just request via email (devaughn@fdaid.org) and a PayPal Invoice will be sent to your email address.

📅 How It Works:

1. Purchase access here on Gumroad
2. You’ll receive a Zoom link by email within 24 hours
3. Show up ready to learn, ask questions, and sharpen your compliance strategy

📩 Questions?
Email: devaughn@fdaid.org

Your validation report should speak for itself. Let’s make sure it says the right things.
#FDA #GMP #CleaningValidation #PharmaTraining #Validation #QualityAssurance #MicroWorkshop