Pharmaceutical Stability Testing

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  • Published date: January 15, 2020
    • Shirley, New York, United States

The purpose of these two programs is intended to identify the likely degradation products which further helps in determining the intrinsic stability of the molecule, establishing degradation pathways, and validating the stability indicating procedures. The conditions used in forced degradation are more severe than those in accelerated degradation. We have the flexibility to set up the standard and non-standard temperature/humidity conditions upon request, as well as freeze/thaw cycle studies. .

Jerry Carter
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