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Pharmaceutical Reference Standards

For decades LGC has supported the pharmaceutical community with more than 10,000 high-quality 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 range of more than 5,000 Mikromol 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 their suitability for both qualitative and quantitative analysis.

Our CoAs provide a complete description of the material they relate to, alongside a summary of the analyses undertaken during the characterisation process - covering assay, purity, stability, uncertainty, homogeneity and more. Explore our range of pharmaceutical reference standards below.

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From a single customised material to a fully managed scientific solution. Our scientists can support you with tailored solutions spanning synthesis, analytical services and product design.

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Webinar: Working Standards in Pharma QC

12th November @ 2pm GMT | 3pm CET | 9am EST
Join us to learn practical strategies for establishing and managing working standards that support analytical confidence, regulatory compliance, and efficiency.

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Supporting E&L analysis

Reference standards for extractables, leachables and impurity testing.

Discover the range
  • Custom Services built around your science

    When catalogue products don’t go far enough.

  • Webinar: Working Standards in Pharma QC

    Building confidence across the analytical lifecycle.

  • Supporting E&L analysis

    Address E&L challenges with greater certainty.


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