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Method Development for Quantification and Validation of Host Cell Protein Impurities Using Elisa and Molecular Weight Determination of Therapeutic Monoclonal Antibody Using Sds-Page

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Item type	Current library	Collection	Call number	Status	Date due	Barcode	Item holds
Dissertation	NIMA Knowledge Centre	Reference	615.1901 GHO (Browse shelf(Opens below))	Not For Loan		PDR00730
CD/DVD	NIMA Knowledge Centre	Reference	615.1901 GHO (Browse shelf(Opens below))	Not For Loan		PDR00730-1

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Previous	615.1901 GAT Analytical Method Development and Validation For Impurity Profiling of Sun Peptide and Its Characterization by LC-MS	615.1901 GAT Analytical Method Development and Validation For Impurity Profiling of Sun Peptide and Its Characterization by LC-MS	615.1901 GHO Method Development for Quantification and Validation of Host Cell Protein Impurities Using Elisa and Molecular Weight Determination of Therapeutic Monoclonal Antibody Using Sds-Page	615.1901 GHO Method Development for Quantification and Validation of Host Cell Protein Impurities Using Elisa and Molecular Weight Determination of Therapeutic Monoclonal Antibody Using Sds-Page	615.1901 GOS Fast Protein Liquid Chromatography	615.1901 GUP Development and Validation of Stability Indicating RP-HPLC Method for Fluvoxamine Maleate	615.1901 GUP Development and Validation of Stability Indicating RP-HPLC Method for Fluvoxamine Maleate	Next

Guided by Dr. Priti J. Mehta

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