Please use this identifier to cite or link to this item:
http://hdl.handle.net/10603/484162
Title: | Analytical Method Development and Validation for Impurities in Anti Cancer Molecules and Sartans |
Researcher: | Gopireddy Ramana Reddy |
Guide(s): | Arthanareeswari, M |
Keywords: | Chemistry Chemistry Analytical Physical Sciences |
University: | SRM Institute of Science and Technology |
Completed Date: | 2022 |
Abstract: | Pharmaceutical analysis is an important activity in pharmaceutical development, control, release, and lifecycle management. It is needed to determine the identity, purity, safety, functionality, and stability of pharmaceuticals. Pharmaceutical analysis is a key department in every pharmaceutical development and manufacturing unit. Analytical methods are developed and validated on a regular basis, and the need for new methods and improvements to the existing methods is always there. Pharmaceutical regulators require pharmaceutical firms to submit and maintain data on the qualitative and quantitative attributes of a drug substance, drug products, and drug components. It is of prime importance and a requirement of pharmaceutical regulators newline |
Pagination: | |
URI: | http://hdl.handle.net/10603/484162 |
Appears in Departments: | Department of Chemistry |
Files in This Item:
File | Description | Size | Format | |
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01_title.pdf | Attached File | 246.73 kB | Adobe PDF | View/Open |
02_preliminary page.pdf.pdf | 454.1 kB | Adobe PDF | View/Open | |
03_content.pdf | 383.59 kB | Adobe PDF | View/Open | |
04_abstract.pdf | 244.87 kB | Adobe PDF | View/Open | |
05_chapter 1.pdf | 1.07 MB | Adobe PDF | View/Open | |
06_chapter 2.pdf | 988.5 kB | Adobe PDF | View/Open | |
07_chapter 3.pdf | 4.79 MB | Adobe PDF | View/Open | |
08_chapter 4.pdf | 166.43 kB | Adobe PDF | View/Open | |
09_annexures.pdf | 237.6 kB | Adobe PDF | View/Open | |
80_recommendation.pdf | 359.44 kB | Adobe PDF | View/Open |
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