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A Guide To GLP: Revision history

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26 December 2025

  • curprev 16:0816:08, 26 December 2025 GuillermoNutter talk contribs 5,626 bytes +5,626 Created page with "<br> GLP regulations are mostly concerned with good study protocols and record keeping. The ICH GCP covers things such as the study design, methodology, and data reporting related to clinical trials. Ensures that raw data are documented and recorded. GMP also requires strict quality management, use of good quality raw materials, identifying deviations in product quality, and using reliable testing laboratories. We focus on enhancing value through asset management, effect..."
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