Cleaning Validation Mini Workshop Video
What FDA Expects in a Cleaning Validation Report – Key Components & Compliance Tips (Video)
Run time: 21 minutes
This concise, expert-led training video walks you through the essential elements FDA expects in a compliant cleaning validation program. Whether you're writing a report, preparing for an inspection, or training your team, this mini-workshop covers the critical points—without the fluff.
Presented by former FDA Investigator and pharma executive DeVaughn Edwards, this 21-minute workshop distills what actually matters during inspections.
What’s covered:
- Setting meaningful acceptance criteria
- Swab and rinse method validation
- Recovery studies: why they’re mandatory
- MACO vs. PDE limits—what to use and why
- Worst-case conditions and equipment selection
- Common FDA findings and how to avoid them
Ideal for QA, validation, and compliance professionals in pharmaceutical or biotech companies. Use it as a refresher, internal training module, or FDA inspection prep tool.
🧪 Optional certificate and quiz available for an additional $10—email devaughn@fdaid.org to request.
21-minute video mini-workshop covering what FDA expects in cleaning validation reports—acceptance criteria, swab/rinse validation, MACO vs. PDE, worst-case logic, and more. Ideal for pharma/biotech QA and validation teams. Optional quiz and certificate available. Contact devaughn@fdaid.org