21 CFR Parts 210/211 - Drug GMPs

The GMP 210/211 regulations address issues including recordkeeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling.

This is a great training and information tool to provide all employees with the CFR requirements for Drug, and Combination Products supporting OTC and Ethical manufacturing.

They fit neatly into your pocket. (size 3.75" x 6.25")

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21CFR210211-C-2512317