Pharmaceutical Reference Standards
For decades, LGC has supported the pharmaceutical community by producing thousands of primary reference standards for quality control. Our high quality enables your work to be as accurate as possible, helping you to create better, safer medicines.
Products in our Mikromol range of more than 7,000 pharmaceutical API, impurity and excipient reference standards are all manufactured in an ISO/IEC 17025 and 17034 accredited facility – and come with a comprehensive Certificate of Analysis (CoA), ensuring its suitability for both qualitative and quantitative analysis.
Our CoAs provide a complete description of the material it relates to, alongside a summary of the analyses undertaken during the characterisation process. This covers assay, purity, stability, uncertainty, homogeneity and more.
Explore our range of pharmaceutical reference standards below.
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- CoA: Download CoA Request CoA
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Certificate of Analysis
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