Audit Ready

𝘖𝘯𝘦 𝘥𝘰𝘤𝘶𝘮𝘦𝘯𝘵𝘢𝘵𝘪𝘰𝘯 𝘦𝘳𝘳𝘰𝘳 = ₹50 𝘭𝘢𝘬𝘩 𝘭𝘰𝘴𝘴!

Once upon a time…

I witnessed a team go through one of the toughest audit weeks of their lives:

A single missing initial on a batch record triggered a chain reaction of questions.

A discrepancy between SOP vs logbook entry raised red flags with auditors.

Handwritten corrections without proper justification almost halted product release.

Sure, documentation slip-ups happen in busy pharma plants.
We’re human. Sometimes we forget, miss a step, or write in a rush.

But here’s what I could never understand:

Why does one small error in a document become a ₹50 lakh financial disaster?

In the pharma industry, it’s simple: “If it’s not documented, it didn’t happen.”

That’s why most Form 483s stem from preventable documentation mistakes.

Over the years, I’ve seen these same 5 blunders repeated across teams and sites.

So I created a simple checklist that helps professionals stay audit-ready every single time.

Link to access my free GMP Audit-Ready Guide: https://drive.google.com/file/d/1pXJ289LoctqOhmGKDBB7BmkVuDJflhsY/view?usp=sharing

It’s a lifesaver for anyone in Engineering, QA, QC, Production, RA or compliance.

Let’s not wait for an audit to fix the habits. Start today.