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Publications by Gadela Venkata Radha
Analytical Method Development and Validation for the Estimation of Imatinib Mesylate and Its Dimer Impurity in Pharmaceutical Formulation by Reverse-Phase High-Performance Liquid Chromatography
Asian Journal of Pharmaceutical and Clinical Research
Pharmacology
Pharmaceutical Science
Related publications
Method Development and Validation of Eprosartan Mesylate and Its Impurities Using Reverse Phase High-Performance Liquid Chromatography
International Journal of Current Pharmaceutical Research
Pharmaceutical Science
Development of Analytical Method for Imatinib Mesylate by Ultraviolet Spectroscopy
Asian Journal of Pharmaceutical and Clinical Research
Pharmacology
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High-Performance Liquid Chromatography Analytical Method Validation for Glutaraldehyde and Benzalkonium Chloride in Disinfectants
International Journal of Applied Pharmaceutics
Pharmaceutical Science
Simple Bioanalytical Quantification Method for Simultaneous Estimation of Simvastatin and Ezetimibe in Human Plasma by Reverse-Phase High-Performance Liquid Chromatography Technique
Asian Journal of Pharmaceutical and Clinical Research
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Development and Validation of Residual Solvent Determination by Headspace Gas Chromatography in Imatinib Mesylate API
SN Applied Sciences
The Determination of Cephradine and Cephalexin by Reverse Phase High-Performance Liquid Chromatography.
Journal of Antibiotics
Drug Discovery
Pharmacology
Method Development and Validation of Lopinavir in Tablet Dosage Form Using Reversed-Phase High-Performance Liquid Chromatography
Asian Journal of Pharmaceutical and Clinical Research
Pharmacology
Pharmaceutical Science
Bioanalytical Method Development, Validation and Quantification of Bosentan by High-Performance Liquid Chromatography in Rat Plasma
World Journal of Pharmaceutical Research
Analytical Stability Indicative Method Development and Validation by High Pressure Liquid Chromatography for Assay in Ciprofloxacin Hydrochloride Drug Substances
American Journal of Analytical Chemistry