Out of Specification (OOS) Handling Procedure
Guideline for Handling of Out of Specification (OOS) results occurs during analysis of Raw Material and Pharmaceutical Drug Products (Different stages like - In-process, Bulk, Intermediate, Finished Product & Stability Study Samples) Handling Out of Specification (OOS) Results 1.0 Objective : To lay down the procedure for investigation of Out of Specification (OOS) result(s) that occurs during sample testing in…
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17/02/2021