Stability Testing of Pharmaceutical Products

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  • Published date: September 13, 2021
    • United States

The stability of pharmaceutical products refers to the ability of APIs and preparations to maintain their physical, chemical, biological and microbiological properties. The purpose of stability study is to investigate the changes of the properties of APIs or preparations with time under the influence of temperature, humidity, light and other conditions, so as to provide a scientific basis for the determination of drug production, packaging, storage, transportation conditions and validity. T,C&A Lab runs strictly in accordance with GMP and GLP standards to meet the relevant requirements of compliance, quality, efficiency, etc. We can perform stability testing of pharmaceutical products according to industry standards. Welcome to contact our experts for consultation.

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Tylor Keller
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