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Now showing items 1-20 of 222

Development and validation of new analytical methods for estimation of drugs in their combined dosage forms and validation of gc method for estimation of diethylamine and 2 eha in ampicillin for injection

MISTRI, JANKEE (Parul University, 2011-06-01)

Objective of the research work was “Development and validation of new analytical methods for estimation of drugs in combined dosage forms and validation of available GC method for estimation of diethylamine and 2 Ethyl ...
Process Validation of Solid Dosage Form - Tablet

Rathwa, Minaxi (Parul University, 2011-06-01)

The purpose of research was to study prospective validation of Cimetidine 400 mg tablet dosage formulation. Quality cannot be adequately assured by in-process and finished inspections and testing but it should be built ...
Process Validation Of Cefpodoxime Proxetil Oral Suspension I.P.

Joshi, Priya (Parul University, 2011-06-06)

The aim of this work was to study process validation of cefpodoxime proxetil oral suspension I.P. Three initial process validation batches of same size, method, equipment and validation criteria were taken. The critical ...
Development and validation of uv spectrophotometric and rphplc Methods for simultaneous estimation of esomeprazole Magnesium trihydrate and naproxen in bulk and tablet dosage Form

SUTHAR, JIGARKUMAR (Parul University, 2011-12-01)

NA
Process Validation of Ofloxacin film coated tablet and Diazepam

Goswami, Smita (Parul University, 2012)

The aim of present project work was to carryout Concurrent validation of Ofloxacin film coated tablet and prospective process validation of Diazepam tablet. For concurrent validation of Ofloxacin film coated tablet. Three ...
Development and validation of stability indicating rp-hplc method for simultaneous estimation of sitagliptin and simvastatin in bulk And pharmaceutical dosage form

Patel, Krupali (Parul University, 2012)

Objective: The objective is to develop and validate stability indicating reverse-phase HPLC method for estimation of Sitagliptin and Simvastatin in bulk and pharmaceutical dosage form. Experimental Work: The proposed ...
Analytical Method Development and Validation for Simultaneous Estimation of Cefixime and Azithromycin in Bulk and Their Combined Dosage Form

Rokad, Jenisha (Parul University, 2012)

A simple, accurate and precise UV Spectrophotometric methods and RP-HPLC method was developed and validated for simultaneous estimation of Cefixime and Azithromycin in bulk and tablet dosage form. Two UV spectrophotometric ...
Development and Validation of Stability Indicating RP-HPLC Method for Estimation of Related substances of Cevimeline Hydrochloride in Capsule Dosage Form

Adhvaryu, Harsh (Parul University, 2012)

A specific, accurate, precise, sensitive and stability indicating RP-HPLC method was developed and validated for estimation of related substances of Cevimeline Hydrochloride in Capsule dosage form. The RP-HPLC method showed ...
Development and Validation of Stability Indicating RP-HPLC Method for Simultaneous Estimation of Lafutidine and Domperidone in Bulk and Pharmaceutical Dosage Form.

Chokshi, Pooja (Parul University, 2012)

A sensitive, accurate and precise method was developed and validate for the simultaneous estimation of Lafutidine and Domperidone in capsule dosage form. The RP-HPLC method had shown adequate separation for Lafutidine and ...
Development and Validation of RP-HPLC method for the determination of impurity profile of Desvenlafaxine Extended Release Tablet

SANGHAVI, NEMISH (Parul University, 2012)

A accurate, rapid, precise and specific RP-HPLC method was developed for the determination of impurity profile of Desvenlafaxine in Desvenlafaxine ER tablet. Both known impurities i.e., venlafaxine Base and ODV Dimer ...
Prospective and Concurrent Process Validation of Ranitidine Film Coated Tablet BP 150 mg and Amlodipine Tablet BP 10 mg

Gupta, Neha (Parul University, 2012)

The aim of present project work was to carryout prospective validation of ranitidine film coated tablet BP 150 mg and concurrent process validation of amlodipine tablet BP 10 mg. For both of the process validation , three ...
Method Development and Validation for the Determination of Related Substances of Ezetimibe in Tablet Dosage Form

Maheshwari, Vipul (Parul University, 2012)

The aim of present work was to develop and validate a accurate, precise and sensitive method for the determination of related substances of Ezetimibe in tablet dosage form. The RP-HPLC method has shown adequate separation ...
Development and Validation of Stability Indicating RP-HPLC Method for Simultaneous Estimation of Metoprolol Succinate and Olmesartan Medoxomil in Bulk and Tablet Dosage Form

Savalia, Rajesh (Parul University, 2012)

A simple, accurate, precise and stability Indicating RP-HPLC method was developed and validated for simultaneous estimation of metoprolol succinate and olmesartan medoxomil in bulk and tablet dosage form. The RP-HPLC ...
Development and Validation of UV Spectrophotometric and RP-HPLC Methods for Estimation of Aliskiren Hemifumarate and Valsartan in bulk and Pharmaceutical Dosage Form

Gorwadia, Hitesh (Parul University, 2012)

A First order derivative spectroscopy and RP-HPLC methods were developed and validated for simultaneous estimation of Aliskiren hemifumarate and Valsartan in bulk and synthetic mixture. A simple and easy UV spectrophotometric ...
Development and Validation of Stability Indicating RP-HPLC Method for Simultaneous Estimation of Ofloxacin and Cefpodoxime proxetil in Bulk and Tablet Dosage Form

Patel, Reemaben (Parul University, 2012)

A simple, accurate, precise and stability Indicating RP-HPLC method was developed and validated for simultaneous estimation of ofloxacin and cefpodoxime proxetil in bulk and tablet dosage form. The RP-HPLC method has shown ...
Development and validation of stability indicating rp-hplc method for estimation of related substances of esomeprazole in capsule dosage form

Patel, Chinmay (Parul University, 2012)

A sensitive, accurate and precise method has been developed for the estimation of related substances of Esomeprazole in capsule dosage form. The RP-HPLC method has shown adequate separation for Esomeprazole and its Impurities ...
Development & Validation of UV-Spectroscopic & RP-HPLC Method for Simultaneous Estimation of Levosulpiride & Rabeprazole Sodium in bulk and tablet dosage form

Thakkar, Divya (Parul University, 2012)

A simple, accurate and precise UV Spectrophotometric methods and RP-HPLC method have been developed and validated for simultaneous estimation of Levosulpiride and Rabeprazole Sodium in bulk and tablet dosage form. Two UV ...
Stability Indicating RP-HPLC Method Development and Validation for Psychostimulant Drugs in Syrup Dosage Form

Patel, Krupaben (Parul University, 2012)

A Stability Indicating RP-HPLC method was developed and validated for estimation of Psychostimulant drugs in syrup dosage form. The RP-HPLC method has shown adequate separation of drug A from its degradation products. The ...
Development and Validation of RP-HPLC Method & Dissolution Profiling of Tianeptine Sodium in its Pharmaceutical Dosage Form

Vadgama, Bhumit (Parul University, 2012)

The purpose of this work is to develop a sensitive, selective, and validated RP-HPLC assay of Tianeptine Sodium in bulk drug and tablet form. Tianeptine Sodium was analyzed on INERTSIL ODS C18 column using isocratic ...
Process validation of Pantoprazole and Rabeprazole Lyophilized Product

Desai, Avni (Parul University, 2012)

Since process validation is essential for fulfillment of regulatory requirements and quality, the prospective validation of the new manufacturing process of lyophilized Pantoprazole and Rabeprazole injections I.P was carried ...

Now showing items 1-20 of 222

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