LGC 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, calibrations, drug substance and dru...

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 severa...

Designed to deliver the highest accuracy and reliability, Mikromol excipient standards are primary quantitative standards that are suitable for calibration, assay development or as working standards. Most of the 170+ excipient products in our range are ISO 17034 accredited, and all are supplied with de...

At our reference standards manufacturing site in Luckenwalde, Germany, we have produced high quality API, impurity and excipient reference standards for the pharmaceutical industry for over 28 years. These reference standards are used by our customers for method development and validation, as well as in critical quality control applications. We're accredited to ISO/IEC 17025 and GMP, and a range of our standards are manufactured under ISO 17034. We are experts in a wide range of analytical techniques – from NMR through to HRMS, UPLC and Elemental Analysis. Our expansive site is also the heart of LGC's global distribution network. From here we supply high quality reference standards to thousands of customers worldwide.  Enjoy this view inside the workings of our Luckenwalde site!