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Custom reference standards

Custom reference standards
Product Description

Creating pharmaceutical reference standards to customer specification has always been at the heart of the Mikromol business. We understand that you are constantly discovering new actives and impurities of interest – each year, our dedicated, highly-qualified customs team produces several hundred new materials to fulfil the individual impurity profiling and API qualification needs of customers all around the world – including requests for novel compounds not yet found in our extensive stocked offering or adapted analytical methods and specifications to address your specific application.

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LGC

  • GB
  • 2015
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
Other
View company profile
Categories
more categories Show less

LGC

  • GB
  • 2015
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
Other
View company profile

More Products from LGC (4)

  • Excipient and Concomitant component standards

    Product Excipient and Concomitant component standards

    Designed to deliver the highest accuracy and reliability, Mikromol excipient standards are primary quantitative standards that are suitable for assay development or as working standards. Most of the 170+ excipient products in our range are ISO 17034 accredited, and all are supplied with detailed COAs featu...
  • Impurity reference standards (including a broad range of degradation products)

    Product Impurity reference standards (including a broad range of degradation products)

    Impurities are always present in a therapeutic substance and can significantly alter a drug’s effects on the patient, potentially putting their health at risk. Legislators and official bodies, therefore, set limit and threshold values as well as guidelines requiring the detection, identification, quantific...
  • Primary API reference standards

    Product Primary API reference standards

    Mikromol reference standards for Active Pharmaceutical Ingredients (APIs) are primary quantitative standards – the majority accredited to ISO 17034 and designed to ensure the highest analytical accuracy and reliability. Their intended use is for potency assessments, drug substance and drug product release ...
  • Reference Materials Management

    Product Reference Materials Management

    To support you in bringing even safer medicines to the market, we go far beyond supplying you with the right reference standards. From impurity profiling and working standards outsourcing services, all the way to managing inventory and logistics of your reference standards, we’re fully equipped to provide ...

LGC resources (4)