Many impurities may arise during shipment or shelf life of drug products. Therefore, to perform the stability studies are important to evaluate, predict, and make sure the product safety. Stability in sample package, stability in the marketing package, the stability of the formulation, and stability in delivery package, These are all considered for the stability of the drug product and it is significant to make sure that each has to know the significance of stability studies. The impurity related to the fall is to determine how many potential impurities are actually formed in the process of manufacturing and which is under the storage conditions. Throughout the development stage, this information can be utilized to process to modify in an attempt to reduce the impurities. Also, the stability characteristics information can be utilized for packaging, storage and environmental conditions of drug substance so that unacceptable degradation can be reduced or eliminated.
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