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1 Development and validation of RP HPLC method for simultaneous determination of picroside I, picroside II, phyllanthin and boeravinone B in a polyherbal hepatoprotective tablet formulation    Abstract | Fulltext
2 Development and validation of a novel chemiluminescent immunoassay for diagnosing primary aldosteronism    Abstract | Fulltext
3 HPTLC method development and validation for the determination of andrographolide in raw material and tablet containing ethyl acetate fraction of Andrographis paniculata    Abstract | Fulltext
4 Development and validation of spectrophotometric and spectrofluorimetric methods for determination of cilnidipine    Abstract | Fulltext
5 Development and validation of a chromatographic method for quantification of rasagiline in human plasma    Abstract | Fulltext
6 Development and validation of a spectroscopic method for the simultaneous analysis of miconazole nitrate and hydrocortisone acetate in pharmaceutical dosage form    Abstract | Fulltext
7 Novel ratio subtraction and isoabsorptive point methods for determination of ambroxol hydrochloride and doxycycline in their combined dosage form: Development and validation    Abstract | Fulltext
8 Development and validation of reverse phase high performance chromatography method for determination of olanzapine in microsample rat plasma: Application to preclinical pharmacokinetic study    Abstract | Fulltext
9 Development and validation of reversed phase high performance liquid chromatographic method for determination of amlodipine    Abstract | Fulltext
10 Development and Validation of Improved Method for Fingerprint Analysis of Rhizoma Chuanxiong by Capillary Zone Electrophoresis with Ultraviolet-Diode Array Detection    Abstract | Fulltext
11 Gradient High Performance Liquid Chromatography Method Development and Validation for Simultaneous Determination of Phenylephrine and Ibuprofen in Tablet Dosage Form    Abstract | Fulltext
12 Development and Validation of a Stability-Indicating LC-UV Method for Simultaneous Determination of Ketotifen and Cetirizine in Pharmaceutical Dosage Forms    Abstract | Fulltext
13 Development and Validation of Liquid Chromatography-Mass Spectroscopy/Mass Spectroscopy Method for Quantitative Analysis of Naproxen in Human Plasma after Liquid-Liquid Extraction    Abstract | Fulltext
14 Development and Validation of a RP-HPLC Method for Assay of Atorvastatin and its Application in Dissolution Studies on Thermosensitive Hydrogel-Based Nanocrystals    Abstract | Fulltext
15 Development and Validation of Analytical Method for Losartan-Copper Complex Using UV-Vis Spectrophotometry    Abstract | Fulltext
16 Development and Validation of a Stability-Indicating RP-HPLC Method for Simultaneous Determination of Paracetamol, Tramadol HCl and Domperidone in a Combined Dosage Form    Abstract | Fulltext
17 Development and Validation of a New RP-HPLC Method for the Determination of Aprepitant in Solid Dosage Forms    Abstract | Fulltext
18 Development and Validation of a Dissolution Test Method for Artemether and Lumefantrine in Tablets    Abstract | Fulltext
19 Development and Validation of a Bioanalytical Method for Direct Extraction of Diclofenac Potassium from Spiked Plasma    Abstract | Fulltext
20 Development and Validation of a RP-HPLC Method for the Simultaneous Determination of Rifampicin and a Flavonoid Glycoside - A Novel Bioavailability Enhancer of Rifampicin    Abstract | Fulltext
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