We offer an extensive catalogue (more than 4000 impurities) for immediate shipment. Where stock is unavailable, we will undertake production of new impurities upon customer request. An uncompromising level of quality is offered for each impurity standard provided. Every standard produced is accompanied with a complete Certificate of Analysis (COA) and supported by comprehensive analytical data. We listen carefully to the concerns and needs of customers, and address each promptly and efficiently. We have a facility which follows GLP/GMP and is accredited by ISO 9001:2015, ISO 17025 especially for impurity synthesis. We also offer Primary Reference Standards of United States Pharmacopoeia (USP), European Pharmacopoeia (EP), British Pharmacopoeia (BP), Japanese Pharmacopoeia (JP), Indian Pharmacopoeia (IP) at very competitive prices.
We have considerable expertise in the identification and isolation of new and challenging degradants and unknown impurities. We can provide expert advice on the mechanism of degradant formation and advise on modifications to formulations to reduce their levels. We can even design synthesis of these degradants in cost effective manner to reduce the project cost of our client.
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