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

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Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 250
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PreviewIssue DateTitleAuthor(s)
May-2024Characterization of Monoclonal Antibody (mAb - 1) by Different Analytical Methodologies and Estimation of Bioactives in Leaves of Stevia Rebaudiana Samples by HPTLC MethodKhandhara, Vihar
May-2024Development and Validation of RP-HPLC and UV Spectroscopic Method For Simultaneous Estimation of Dapagliflozin Propanediol Monohydrate and Linagliptin in Synthetic MixtureOza, Nilay A
May-2024Characterization of IgG4 Monoclonal Antibody Using Various Analytical Techniques for Quality Assessment of Upstream and Downstream Process Sample and Method Development and Validation of Trastuzumab by Hydrophobic Interaction ChromatographySamdani, Jinal
May-2024Green Analytical Method Development and Validation of Levobupivacaine Hydrochoride by RP-HPLCParmar, Janvi
May-2024Green Analytical Method Development and Validation of Atenolol by HPLC and HPTLCHerma, Cyrus
May-2024Conventional and Microwave Assisted Degradation Study of Drug-Excipients Using High-Performance Liquid Chromatography and Microwave-Assisted Degradation Study of Drug-Excipients Using High-Performance Thin Layer ChromatographyAnand, Asit N
May-2024Method Development and Forced Degradation for SUN ® Peptide Using RP-HPLCGandhi, Achal
PDR00850_22MPH812.pdf.jpgMay-2024Regulatory Requirement and Re-Registration of Pharmaceutical Products in the Republic of MoldovaPatel, Yesha
PDR00849_22MPH811.pdf.jpgMay-2024Regulatory Compliances for Food and Nutraceuticals in USAKalola, Utsav
PDR00848_22MPH810.pdf.jpgMay-2024Generic Drug Product Registration in Ukraine to Align with the EMA Regulation: A Case Study of Mycophenolate Mofetil and Module 3 CTD Preparation for SubmissionModi, Sharvil
PDR00847_22MPH809.pdf.jpgMay-2024Proton Therapy and It's Regulatory Framework in IndiaSingh, Ruchi
PDR00846_22MPH808.pdf.jpgMay-2024Image Oncology: A Regulatory PerspectiveAdodariya, Meet
PDR00845_22MPH807.pdf.jpgMay-2024Regulatory Strategies and Requirements for Registration of Innovator Drug Products Entering Latam Contries: Mexico, Peru, Equador and ChileKulkarni, Mandar Arvind
PDR00844_22MPH806.pdf.jpgMay-2024Formal Meetings Between USFDA and Applicants of Complex Products Under GDUFA and PDUFAShah, Khushi
PDR00843_22MPH805.pdf.jpgMay-2024Comparative Study on Current Regulatory Requirements for Generic Synthetic Peptide Based Drug-Device Combination Products in U.S. and EuropePandya, Khushi
PDR00842_22MPH804.pdf.jpgMay-2024Post-Approval CMC Changel in Brazil and EuropeShah, Gaurang
PDR00841_22MPH803.pdf.jpgMay-2024Regulatory Pathway for Registration of ORS with Zinc in Domestic Market and its Comparison with African Countries and The Regulatory Perspective of Real-World Data in the US, Europe, and the UKVaghela, Gargi
PDR00840.pdf.jpgMay-2024A Comparison of Variation Filling Approaches in South Africa and Botswana’s Legal FrameworkDesai, Drashti
PDR00839.pdf.jpgMay-2024Preparation and Validation of CTD and eCTD for an ANDA of a Model Tablet as per USFDA RequirementsPatel, Aneri
PDR00796_21MPH304.pdf.jpgMay-2023In-Vitro Drug Release of Dolutegravir Sodium, Lamivudine and Tenofovir Fumarate Tablet by RP-HPLC Analysis from its Combined Dosage Form and Microwave Assisted Hydrolytic Degradation of Fluconazole and its Comparison with Conventional Heating Method using RP-HPLCHariyani, Heer
Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 250
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