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"How to Avoid GMP Audit Failures"

eBook

FDA inspectors repeatedly cite the same problems: missing written procedures, lapses in laboratory controls, and inadequate investigations of discrepancies. Despite years of warnings, these problems still prompt most warning letters, delays, and costly remediations.

Download this ebook from Agilent to dive into the data behind these failures and gain practical guidance and advice for documentation that best serves real-world GMP environments.

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