With our expertise in Development and Manufacturing of Active pharmaceutical Ingredients in the domain of High Potent APIs as well Bulk actives and intermediates, Scintel extends our service for synthesis and profiling of API Impurity Standards, In Process Impurities, Degradation Impurities and complex Nitrosamine impurity standards. Every Impurity comprises with COA, Purity by HPLC or GC, 1H- NMR,C13-NMR, Mass, FTIR, Ash content or Potency by TGA and MSDS. Additional Data like Q-NMR,CHNS,UV and RRF can also be given based of requirement. We also provide Technical justification Report for impurities which are hard to synthesis or non-feasible by chemical route of synthesis. The Technical project report comprises of supporting Analytical Data and Technical justification.