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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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With limited regulatory guidance on impurity reference standards (IRSs), this paper provides expert-backed recommendations for IRS characterisation across a variety of applications.

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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.

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  • Special Promotion: Get 4 x 25mg for the price of 2

    Take advantage of this great offer while stock lasts!

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    Characterising Non-Compendial Impurity Standards: What Is ‘Good Enough’?

  • Extractables and Leachables

    reference materials


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