Case Study: Mislabeling Due to Confusion Between Re-Test Date and Expiry Date
In pharmaceutical manufacturing, the distinction between “re-test date” and “expiry date” is critical. Confusing these two can result in serious GMP violations, product recalls, and regulatory action. This case study explores a real-world scenario where an active pharmaceutical ingredient (API) was mislabeled due to this very confusion, leading to a failed regulatory audit and triggering…
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