From the qualification of Active Pharmaceutical Ingredients (APIs), to identification of elemental impurities, to the determination of the sterility of end products, reference materials are a critical component for the pharmaceutical manufacturer to ensure the production of a safe and high quality drug material. We offer a vast portfolio of reference materials to meet the needs of your analytical workflow in the drug manufacturing process. Whether you require a Compendial Primary Standard from the most widely used Pharmacopeia, a replacement for your currently in-house manufactured Secondary Standards, or to quantify potential elemental impurities, we are your partner in helping you deliver accurate results, meet regulatory demands and keep drug materials safe. Our high standards match yours!