ConsultWise › Documents › Quality Control
In a current Good Manufacturing Practice (cGMP) environment, maintaining a "State of Control" is a fundamental regulatory requirement.
The full text is not reproduced here. Preview any document free on the catalog page, then buy the complete catalog in your language.
| Document type | Code |
|---|---|
| SOP | SOP-QC-027 |
| Form | FRM-QC-030 |
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.
Every document is a customizable template supplied for the buyer's own review and adaptation. ConsultWise is not a regulatory authority and does not guarantee any inspection or audit outcome.