LGC Colour Standards for Pharmaceutical Product Testing
Colour is a critical quality attribute (CQA) in pharmaceutical development and manufacturing, providing essential information on product identity, batch-to-batch consistency, and stability across dosage forms. International pharmacopeias – including the United States Pharmacopeia (USP) and the European Pharmacopoeia (Ph. Eur.) – define standardised methodologies and acceptance criteria for colour assessment. These encompass both visual comparison and instrumental analysis using colour reference standards, as specified in USP <631> USP <1061> and Ph. Eur. 2.2.2.
LGC Standards’ colour reference materials that are manufactured and tested according to USP and EP ensure accuracy, consistency, and full traceability – so you can test with confidence and meet pharmacopoeial requirements every time.
LGC standards
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Country/Region:United Kingdom
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On CPHI since:2015
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Certificates:1
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Employees:1000 - 4999
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