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The strategic importance of this Standard Operating Procedure (SOP) lies in the preservation of biological sample integrity and the mitigation of regulatory risk during the transport of microbial isolates.
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| Document type | Code |
|---|---|
| SOP | SOP-PKG-001 |
| Form | FRM-PKG-001 |
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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