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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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Everything on one site!

View our complete solution to your laboratory’s needs – from research, drug design and development to manufacturing and qualification.

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Extractables and Leachables

Our high-quality range of materials supports your extractable and leachable testing, enabling confidence in the integrity of both your results and product.

Discover now
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Elemental impurities

Each of the standards that LGC produces for USP <232> and ICH Q3D compliance meets the stringent requirements of ISO 17034 and ships with a comprehensive Certificate of Analysis.

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  • Everything on one site!

    TRC research chemicals are now fully available at lgcstandards.com

  • Extractables and Leachables

    reference materials

  • Elemental impurities

    certified reference materials


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