1. DSpace at Nirma University
  2. 04. Institute of Pharmacy
  3. Department of Pharmaceutical Analysis

M.Pharm. Research Reports, Pharmaceutical Analysis : [250] Collection home page

Browse
Subscribe to this collection to receive daily e-mail notification of new additions RSS Feed RSS Feed RSS Feed
Collection's Items (Sorted by Submit Date in Descending order): 161 to 180 of 250
< previous   next >
PreviewIssue DateTitleAuthor(s)
PDR00452.pdf.jpgMay-2017Developement and Validation of a Stability Indicating RP-HPLC Method for Determination of Macitentan in Bulk DrugBavishi, Bhaumik Rajendra
PDR00364.pdf.jpgMay-2015Electronic Common Technical Document (ECTD) Filing in Europe and Comparative Study of Dossier Requirements for Generics Across US, Europe, Australia and New ZealandRichardson, Vanessa James
PDR00363.pdf.jpgMay-2015Regulatory Landscape for Oral Solid Dosage Form of Dossier Filing in USA and Its Comparison with Canada and EULunia, Twisha
PDR00360.pdf.jpgMay-2015Annual Product Quality Review: As A Quality Enhancement Tool and Its Regulatory PerspectiveKanojia, Meet Sanjay
PDR00358.pdf.jpgMay-2015Registration Process of Drug and Dossier Filing in Russia and Its Comparison with Others CIS Countries and IndiaPatel, Gayatri
PDR00357.pdf.jpgMay-2015Comparison of Checklist and Legal Document Generic Pharmaceutical Drug in Emerging Market and Preparation of X Drug Dossier for Vietnam CountryRajpurohit, Dushyant
PDR00347.pdf.jpgMay-2015Bio-Analytical Method Development and Validation of RP-HPLC Method For the Simultaneous Estimation of Drotavarine Hydrochloride and Mefenatic Acid in Human Plasma by Applying Design of Experiment ApproachPatel, Vaibhavi
PDR00346.pdf.jpgMay-2015Bio-Analytical Method Development and Validation of Gamma-Oryzanol in RAT Plasma and Brain Homogenate Using Reversed Phase-High Performance Liquid ChromatographySingh, Sumit Kumar
PDR00342.pdf.jpgMay-2015Development and Validation of Spectrofluorimetric Methods for Estimation of Tramadol Hydro chloride in Human PlasmaPrajapati, Krina
PDR00395.pdf.jpg2016Regulatory Requirements for Registration for Active Pharmaceutical Ingredients in Europe with Comparision to USPatel, Sweeti
PDR00394.pdf.jpg2016A Comprehensive Study for The Regulations of Genotoxic Impurities in Pharmaceutical Drug Substances & Products with Special Reference to Their Detection, Identification and EvaluationeJain, Shashank
PDR00393.pdf.jpg2016Comprehensive Study on Regulatory Requirement for Biosimilars in Egypt and Its Comparision with Europe, U.S. and CanadaPatel, Rushviben J.
PDR00392.pdf.jpg2016Comperative Study of African and ASEAN Regulatory Framework and Registration Requirements for Generic DrugsWarier, Nandini S.
PDR00391.pdf.jpg2016Registration Requirements and Comparative Study of Genetic Drug Registration Between MENA and ASEAN CountriesVaishnav, Mohak P.
PDR00390.pdf.jpg2016ANDA Dossier Filing in US Market for "X" DrugRajpurohit, Manisha
PDR00389.pdf.jpg2016Regulatory Landscape of 505(b)(2) Application for Parenteral Dosage Form in USA & Case Studies for Parenteral Dosage Form: Deviations and CAPA in Pharmaceutical IndustryShah, Kavina J.
PDR00388.pdf.jpg2016Regulatory Comparision Study Between Europe and Australia for Generic Medicines with Special Focus on Filing Requirements, Pre-Approval and Post-Approval ProcessesSarkar, Debashish
PDR00387.pdf.jpg2016Post Approval Regulatory Compliance Management for Generics in U.S. MarketDoshi, Chandni
PDR00386.pdf.jpg2016Analytical Method Development and Validation of Estimation of Vitamin E Acetate From Multi-Vitamin Dosage From Quality by Design(QbD) ApproachPatel, Zalak V.
PDR00385.pdf.jpg2016Quality by Design Based Development and Validation of Stability Indicating HPLC Method for Simultaneous Estimation of Chloropheniramine Maleate and Dextromethorphan Hydrobromide in Syrup FromulationDesai, Sneha
Collection's Items (Sorted by Submit Date in Descending order): 161 to 180 of 250
< previous   next >

Discover