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

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Collection's Items (Sorted by Submit Date in Descending order): 61 to 80 of 250
PreviewIssue DateTitleAuthor(s)
PDR00723_20MPH801.pdf.jpgMay-2022Post-Approval Management of An Anda Approved Drug ProductBhardwaj, Aakash
PDR00722_20MPH313.pdf.jpgMay-2022Development and Validation of Analytical Method for Estimation of Aspirin and Dipyridamole in Their Fixed Combine Dosage FormPatel, Vishwa A
PDR00721_20MPH311.pdf.jpgMay-2022Development and Validation of Stability Indicating HPLC Method For Estimation of Diroximel FumarateShah, Shikha S
PDR00720_20MPH308.pdf.jpgMay-2022Development of LFIA Based Sandwich ELISA Method For Detection of Aflatoxin and It’s Comparision With HPLC MethodPatel, Nipa
PDR00719_20MPH305.pdf.jpgMay-2022Development and Validation of Stability Indicating RP-HPLC Method For Simultaneous Quantification of Vildagliptin and Metformin Hydrochloride In Their Bulk Dosage FormDesai, Kashish J
PDR00718_20MPH303.pdf.jpgMay-2022Analytical Method Development and Validation For Impurity Profiling of Sun Peptide and Its CharacterizationGatlewar, Bhagwati D
PDR00717_20MPH302.pdf.jpgMay-2022Development and Validation of Stability Indicating RP-HPLC Method For Quantification of Baclofen and Its Related Substance In Tablet Dosage FormPatel, Avani
PDR00698_19MPH807.pdf.jpgMay-2021Regulatory Submission for Anda Dossier Filing and Current Impact of Gdufa ActSeervi, Prakash
PDR00697_19MPH803.pdf.jpgMay-2021Identification and Implementation of Product Specific Standard For Orthopedic DeviceBariya, Divyesh
PDR00694_19MPH308.pdf.jpgMay-2021Method Development and Validation of Reverse-Phase HPLC for Purity Analysis and Size-Exclusion HPLC for Aggregate Analysis of Monoclonal Antibody, SUNmAbRamnani, Khushboo
PDR00693_19MPH302.pdf.jpgMay-2021Validation and Assessment of The Stability Indicating capability of a CEX-HPLC For Charge Variant Analysis And a SEC-HPLC Method For size Heterogeneity Analysis of a Monoclonal Antibody; SunmabSaxena, Ashutosh
PDR00685_19MPH305.pdf.jpgMay-2021Validation and Assessment of Stability Indicating RP-HPLC Method For Salbutamol Sulfate in Inhalational Solution and Forced Degradation StudyKhanuja, Harmeet Singh
PDR00682_19MPH813.pdf.jpgMay-2021Preparation of Modul3-IIIContent for Sirolimus Polymeric Nanoparticles' (ANDA Product RAPCIN 1MG) Approval Process in USA and INDIAPatel, Khushboo
PDR00681_19MPH812.pdf.jpgMay-2021Regulatory Submission For Post Approval Variations in SEurope To Maintain Product Life Cycle Via SoftwareMaheshwari, Manali
PDR00680_19MPH811.pdf.jpgMay-2021Regulatory Requirements For Registration of Drug Products in African MarketDesai, Vishwa
PDR00679_19MPH810.pdf.jpgMay-2021Regulatory Perspective on Technology TransferSrivani, Yellamraju Sravya
PDR00678_19MPH809.pdf.jpgMay-2021Variation To Register Manufacturer of Bi-Component Antihypertensive Drug As A Part of Mutual Recognition Procedure In EuropePamecha, Shubhi
PDR00677_19MPH808.pdf.jpgMay-2021Regulatory Requirements And Comparative Study Of Veterinary Products In Kenya, Tanzania, Uganda And South AfricaKathiria, Prutha Nanubhai
PDR00676_19MPH806.pdf.jpgMay-2021Regulatory Landscape For Drug Registration Requirements and Procedure In China: An Emerging Pharmaceutical MarketDoshi, Mohit
PDR00675_19MPH805.pdf.jpgMay-2021Regulatory Requirements and Comparative Study of Cosmetics In Vietnam, Malaysia, Singapore, Philippines (Asean Countries) and Sri LankaVadera, Kushal
Collection's Items (Sorted by Submit Date in Descending order): 61 to 80 of 250