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Titlebook: Drug Stability and Chemical Kinetics; Muhammad Sajid Hamid Akash,Kanwal Rehman Book 2020 The Editor(s) (if applicable) and The Author(s),

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21#
發(fā)表于 2025-3-25 04:46:51 | 只看該作者
Role of Microbial Degradation on Drug Stability,croorganism is more common in untreated raw materials during the process of manufacturing. The most common reason of contamination is high microbial and fungal count in those pharmaceutical products that contained naturally derived raw materials. Visual appearance of pharmaceuticals is also affected
22#
發(fā)表于 2025-3-25 08:37:56 | 只看該作者
23#
發(fā)表于 2025-3-25 11:49:09 | 只看該作者
Analytical Techniques for the Assessment of Drug Stability,l role for this purpose. In this chapter, we have discussed various analytical techniques and methodologies for the assessment of the drug’s quality and stability. The chapter highlights a range of analytical methods, i.e., chromatographic, electrochemical, electrophoretic, spectroscopic, and titrim
24#
發(fā)表于 2025-3-25 19:21:39 | 只看該作者
25#
發(fā)表于 2025-3-25 23:57:03 | 只看該作者
26#
發(fā)表于 2025-3-26 03:12:42 | 只看該作者
Stability Studies of Extemporaneous Pharmaceutical Products,oral liquid dosage forms are most commonly prepared extemporaneously among all these preparations. The stability of extemporaneous preparations is highly critical; hence the formula utilized for extemporaneous dispensing should be preferably validated and have sufficient stability evidence. Each ext
27#
發(fā)表于 2025-3-26 04:41:32 | 只看該作者
28#
發(fā)表于 2025-3-26 09:39:33 | 只看該作者
https://doi.org/10.1007/3-540-08253-0cution of stability studies on both drug and dosage form. The aim of these guidelines is not to constrain the experimentation but to execute the proper and meaningful experiments. The scope of these guidelines is limited to pharmaceutical dosage forms and any feed impregnated with medicinal product.
29#
發(fā)表于 2025-3-26 15:21:12 | 只看該作者
30#
發(fā)表于 2025-3-26 19:38:45 | 只看該作者
Waves on Water of Variable Depthcroorganism is more common in untreated raw materials during the process of manufacturing. The most common reason of contamination is high microbial and fungal count in those pharmaceutical products that contained naturally derived raw materials. Visual appearance of pharmaceuticals is also affected
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