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In a current Good Manufacturing Practice (cGMP) environment, the implementation of a formalized calibration program is a strategic cornerstone for maintaining a state of control and ensuring the highest standards of data integrity.
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| Document type | Code |
|---|---|
| SOP | SOP-QC-006 |
| Form | FRM-QC-006 |
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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