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The primary objective of this Standard Operating Procedure (SOP) is to establish a rigorous framework for identifying and managing objectionable microorganisms at the [Your Company] to ensure absolute product safety and regulatory compliance.
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| Document type | Code |
|---|---|
| SOP | SOP-QC-008 |
| Form | FRM-QC-008 |
FDA 21 CFR 210/211 and Part 11, EU GMP (EudraLex Volume 4, including Annex 1 and Annex 11), ICH Q7–Q12, and WHO GMP. Supplied in 13 languages.
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