Conductivity Analysis of Pharmaceutical Water Systems

What this document is for

In the production of pharmaceutical products, the chemical purity of water is a critical quality attribute (CQA) that directly impacts product safety, stability, and efficacy. Conductivity testing serves as a primary analytical method to monitor this purity by detecting the presence of ionic contaminants.

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Grounded in

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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