$45

Cleaning Validation Mini Workshop Video

Buy this

Cleaning Validation Mini Workshop Video

$45

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.

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Watch link provided after purchase

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

Product Type
Training Video
Topic
Pharmaceuticals, Biotech, Contract Manufacturing Organizations (CMOs)
Use Case
Internal Training, Inspection Prep, Report Support, QA Refresher
Created By
Former FDA Investigators
Delivery Format
Video Download
Run Time
21 minutes
Includes
Full Video Training, Compliance Walkthrough, Worst-Case Examples
Level
Intermediate
Add-Ons Available
At additional cost (contact devaughn@fdaid.org
Size
1.85 GB
Duration
21 minutes
Resolution
1080p