Analytical Methods in Pharmaceuticals
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Scope of this subject
This cluster of papers focuses on the development and validation of green analytical chemistry methods for pharmaceutical analysis. It includes topics such as the validation of HPLC methods, stability indicating assays, forced degradation studies, impurity profiling, and the use of spectrophotometric methods. The cluster emphasizes the importance of environmentally friendly analytical procedures in pharmaceutical analysis.
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Research vocabulary
pharmaceutical analysis; method validation; pharmaceutical quality control; simultaneous determination; drug stability; tablets; stability-indicating assay; human plasma; analytical method validation; spectrophotometric determination; pharmaceutical dosage forms; degradation products; reversed-phase HPLC; simultaneous estimation; RP-HPLC method development; HPLC method development; plasma drug quantification; HPLC method validation; pharmaceutical preparations; forced degradation; impurity determination; UV detection; bioanalytical method validation; ICH guidelines; UV spectrophotometry
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Numeric address and provenance
Morton address: 36183005873702993 · morton4x16-v1
Coordinates: (3, 16, 1602, 11460). The address interleaves categorical identifier bits. Nearby addresses are not guaranteed to describe semantically similar subjects.
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