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Stability Testing
 
Stability testing is to certify that the how long a medical devices, pharmaceutical product, chemicals product and pesticide products can be stored without any change in its original chemical composition within prescrived limits.
 
The material and products when stored for long durations there should not be any changes and release byproducts. Stability testing provides evidence on how certain pharmaceutical drugs can be stored at room temperature and in controlled conditions.
 
The physical, chemical and microbial properties of a chemicals, medical devices and pharmaceutical product may change under extreme storage conditions. The shelf-life of a product has been studied during the stability testing under the prsecrived temparature and humidity.
 
Shelf-Life Determination: The quality of a Chemicals, pharmacuticals and medical devices varies with time under temperature, humidity and light intensity. 
The studies show that  how long a product  can be stored at normal and accelerated conditions without any degradation. This study helps to determine the shelf-life of that product. As per the report of the shelf life study, the expiry date of the product to be fixed.
The condition of storage are different products require different storage conditions. In the stability testing lab, storage conditions and changes in the substances are recorded during the evaluation of the study. The stability study, the storage condition is recommended for a particular product.
During the study, each ingredient has been analysed under various environmental factors. Shelf life/Stability testing is a caluculated criteria  to study the effectiveness of a new product. This testing helps to assess the physical, chemical,  therapeutic stability of a product. As per the study, R&D professionals redesign the existing product and develop a new product.
Ensures Quality: Quality assurance is an integral part of the pharmaceutical industry. The product is kept under the influence of high stresses and the rate of decomposition is observed. Stability testing assures the purity of ingredients and the quality of the final product. The stability report ensures that the pharmaceutical product is fit for human consumption. This gives the companies the confidence to launch new products in the market. The chances of product recall may decrease.
Packaging Material Selection: During stability testing, the pharmaceutical product is exposed to humidity and temperature. As per the effect of water activity and temperature on the product, packaging materials are chosen for the product. The ideal container must tolerate the stresses. The packaging should maintain the quality of the product during transportation and storage.
Legal Approvals: Stability testing of the pharmaceutical products is required for regulatory approvals. If a product fails to meet the quality standards prescribed by ICH and WHO, the product will not get approval for commercialization.