- Method validation: A complex concept
- Recent updates on codeine
- Simultaneous estimation of amlodipine besylate and nebivolol hydrochloride in tablet dosage forms by reverse phase-highperformance liquid chromatographic using ultraviolet detection
- A developed and validated stability-indicating reverse-phase high performance liquid chromatographic method for determination of cefdinir in the presence of its degradation products as per International Conference on Harmonization guidelines
- Spectrophotometric estimation of solifenacin succinate in tablet formulations
- Isolation and determination of deoxynivalenol by reversed-phase high-pressure liquid chromatography
- Stress degradation studies and development of a validated stability-indicating-assay-method for determination of diacerein in presence of degradation products
- Development of the UV spectrophotometric method of Olmesartan medoxomil in bulk drug and pharmaceutical formulation and stress degradation studies
- Development and validation of reversed phase– high-performance liquid chromatography method for determination of paracetamol and lornoxicam in tablet dosage form
- Spectrophotometric simultaneous determination of Tenofovir disoproxil fumarate and Emtricitabine in combined tablet dosage form by ratio derivative, first order derivative and absorbance corrected methods and its application to dissolution study
- Spectrophotometric estimation of tamsulosin hydrochloride by acid-dye method
- Simultaneous determination of paracetamol and lornoxicam by RP-HPLC in bulk and tablet formulation
An International, Peer-Reviewed, Open Access Multidisciplinary Pharmacy Journal
