20 must use GMP documentation rules for pharmaceutical laboratory

Imagine you're an employee of a pharmaceutical laboratory responsible for making sure your company's products are safe, pure, effective, and reliable. How do you do it?

To confirm your test results are trustworthy and unbiased, you would turn to well-designed policies, procedures, guidelines, methods, protocols, and all types of records.

There are policies that set the overarching rules, procedures that outline specific steps to follow, guidelines that provide best practices, and manuals that cover everything in between.

There are also forms, logs, and registers to keep track of all the little details, as well as product specifications, analytical methods, manufacturing formulae, calculation of raw data, and more.

The significance of well-designed GMP documentation is immense. Sometimes these are labeled as the “hidden factory”.

In this video, we'll explore GMP documentation rules in pharmaceutical laboratories, why it's important, and how they can be implemented in the pharmaceutical industry.

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