Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/596046
Title: New Synthetic Approach for Manufacturing of Iron Salt and Calcium Salt
Researcher: Jalundhwala Forum
Guide(s): Londhe Vaishali
Keywords: Clinical Pre Clinical and Health
Manufacturing of Iron salt and Calcium salt
Pharmacology and Pharmacy
Pharmacology and Toxicology
University: Narsee Monjee Institute of Management Studies
Completed Date: 2024
Abstract: Indian pharmaceutical industries comprises of a pool of manufacturers involved in manufacturing of ingredients, formulations, primary packaging and supply chain. They are spread across micro, small, medium as well as large enterprises. All of them have to cater to generic quality standards. This makes it challenging for some of the industries to ensure regulatory compliance. The regulators demand paradigm shift from product knowledge to process knowledge. All these, together makes it challenging for the industry to sustain growth. The study aimed at reviewing the literature for the use of operational excellence as a medium to achieve higher regulatory compliance. It reviewed the impact of operational excellence on various pharmaceutical industries, the challenges they would encounter to implement it. Some enablers and driving forces for the implementation of operational excellence were also reviewed. All this together, assisted an organization to plan a roadmap and assess its performance towards operational excellence finally leading to enhanced regulatory compliance. On the basis of this literature review, the rationale of the study was to make active pharmaceutical ingredient (API) manufacturing industry operationally excellent. Here, Quality by Design (QbD) as an approach to synthesize an iron salt and a calcium salt was explored. The primary objective of the study was to find new synthetic approach for the manufacturing of API. The scope of the study was expanded to an iron salt (Ferric ammonium citrate) and a calcium salt (calcium orotate). The secondary objective of the study included theoretical comparison of the new synthetic approach with other conventional methods and find the most operationally excellent one thus, ensuring higher regulatory compliance. The work was first performed on iron salt. Ferric ammonium citrate was the salt under study. The challenges to manufacture this salt were reviewed and QbD approach was applied. Key starting material to manufacture the salt were reviewed.
Pagination: i-vi;184p
URI: http://hdl.handle.net/10603/596046
Appears in Departments:Department of Pharmaceutical Sciences

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01_title.pdfAttached File117.41 kBAdobe PDFView/Open
02_prelim pages.pdf1.2 MBAdobe PDFView/Open
03_content.pdf139.84 kBAdobe PDFView/Open
04_abstract.pdf65.73 kBAdobe PDFView/Open
05_chapter 1.pdf745.24 kBAdobe PDFView/Open
06_chapter 2.pdf558.38 kBAdobe PDFView/Open
07_chapter 3.pdf196.14 kBAdobe PDFView/Open
08_chapter 4.pdf1.65 MBAdobe PDFView/Open
09_chapter 5.pdf2.01 MBAdobe PDFView/Open
10_annexures.pdf3.83 MBAdobe PDFView/Open
80_recommendation.pdf661.83 kBAdobe PDFView/Open
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