saiyog pharmachem integrated growing company of Impurity and impurity standards established with the purpose of serving the pharma industry , is aiming to become one of the fastest growing company in India we specializes in isolation and purification of impurity by preparative HPLC as well as the custom synthesis of Impurity.
we will offer custom synthesis of Manufacturing Impurities as per the requirement of the customer. We will prepare the requested API impurities either by following known literature procedures or synthesis protocols provided by the Client. All impurity standards will be supplied with certificates of analysis (COA) and 1H NMR, Mass, HPLC purity Additional Data CNMR,LCMS,IR ,TGA, will provide by customer request.
To support all global Pharmaceutical ,healthcare , and formulation industry in drugs impurity profile needs for global regulatory market and DMF filling We provide a cost-effective and time-bound research solutions in the area of Impurity synthesis, metabolites synthesis ,custom synthesis, and nalytical development with time line delivery High standards of purity customer satisfaction is our first priority
To become Quality and time bound cost effective service provider for the global pharma industry in Impurity synthesis, metabolites synthesis ,custom synthesis, and analytical development
Regulatory agencies have acknowledged impurities, especially potential genotoxic impurities (PGIs),as a high priority in the drug development approval process. Since impurities found in pharmaceutical drug substances can potentially exhibit pharmacological activity, there are reporting, identification and qualification thresholds dictated by ICH guidelines. Impurity levels need to be understood and controlled for the benefit of safety administering pharmaceutical products to humans. Impurities impact not only the safety of drugs, but also the development time if not addressed early during the scale-up process.