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10Determination of Rufinamide in the Presence of 1-[(2,6-Difluorophenyl)Methyl]-1H-1,2,3-Triazole-4 Carboxylic Acid Using RP-HPLC and Derivative Ratio Methods as Stability Indicating Assays to Be Applied on Dosage Form
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13Ultrahigh-performance liquid chromatography-ultraviolet absorbance detection-high-resolution-mass spectrometry combined with automated data processing for studying the kinetics of oxidative thermal degradation of thyroxine in the solid state
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14Investigation of Reaction Mechanisms of Drug Degradation in the Solid State: A Kinetic Study Implementing Ultrahigh-Performance Liquid Chromatography and High-Resolution Mass Spectrometry for Thermally Stressed Thyroxine
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15Microenvironment Sensitive Charge-Transfer Dye for Tandem Sensing of Multiple Analytes at Mesoscopic Interfaces
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18A Validated RP-HPLC Stability Method for the Estimation of Chlorthalidone and Its Process-Related Impurities in an API and Tablet Formulation
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19Development of High-Throughput Glass Inkjet Devices for Pharmaceutical Applications
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20Pilot scale production, kinetic modeling, and purification of glycine betaine and trehalose produced from Actinopolyspora halophila (MTCC 263) using acid whey: A dairy industry effluent
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21Identification, isolation, and synthesis of seven novel impurities of anti-diabetic drug Repaglinide
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22Regulatory Updates and Analytical Methodologies for Nitrosamine Impurities Detection in Sartans, Ranitidine, Nizatidine, and Metformin along with Sample Preparation Techniques
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23Photocurable Bioink for the Inkjet 3D Pharming of Hydrophilic Drugs
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24Identification, synthesis and quantification of process-related impurities in auraptene
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25Identification, synthesis and quantification of process-related impurities in auraptene
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26Identification, synthesis and quantification of process-related impurities in auraptene
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27Impurity Profiling of Solid Oral Drug Products to Sail through GDUFA-II Requirements
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28Determination of the impurities in drug products containing montelukast and in silico/in vitro genotoxicological assessments of sulfoxide impurity
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29Tools and workflow for structure elucidation of drug degradation products
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30Recent Trends in Product Development and Regulatory Issues on Impurities in Active Pharmaceutical Ingredient (API) and Drug Products. Part 2: Safety Considerations of Impurities in Pharmaceutical Products and Surveying the Impurity Landscape
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31Chromatographic methods for the determination of active substances and characterization of their impurities in pesticide formulations
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32Veteriner Tibbî Ürünlerde Safsizliklar
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