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Pharmaceutical impurity reference standards are used by pharmaceutical manufacturers to accurately quantify manufacturing and degradation impurities present in their finished Active Pharmaceutical Ingredients (API’s) . The custom synthesis of pharmaceutical impurities can be challenging and involves many steps. FB Pharmtech have been carrying out the custom synthesis of pharmaceutical impurity reference standards for over 12 years and have provided impurities to our customers all over the world, including providing bulk impurity reference standard to many of the leading global impurity providers.