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The integrity of water utility systems is fundamental to the safety and efficacy of pharmaceutical products. Because water serves as a primary solvent and cleaning agent in drug manufacturing, stringent testing protocols are required to mitigate the risk of chemical contamination.
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| Document type | Code |
|---|---|
| SOP | SOP-QC-014 |
| Form | FRM-QC-014 |
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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