Modern Aspects of Pharmaceutical Quality Assurance (PDF)
Developing & Proposing Application models, SOPs, practical audit systems for Pharma Industry
(Sprache: Englisch)
The pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial...
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The pharmaceutical quality system ensures that the process performance is suitably achieved, the product quality is regularly met, improved opportunities are identified and evaluated, and the knowledge is constantly expanded. Auditing also plays a crucial role within the pharmaceutical industry. It helps to assess and review quality to improve and build a better system for the benefit of companies.
The chapters cover the various aspects of Pharmaceutical Quality Assurance. The selection of topics is mainly based on the requirements of Pharmaceutical regulatory guidelines of India, the UK, the USA, Australia, and South Africa. Each chapter includes the abstract, detailed explanation, implementation guidelines, flowcharts, layouts, and Standard Operating Procedure of quality metrics for the Pharmaceutical Manufacturing System
This book aims to develop a tool that will substantially decrease the number of Inspectional Observations and Warning letters, thus eliminating Import Alerts and Consent Decree. This book targets the Pharmaceutical Industry and students of Pharmaceutical Quality Assurance so they can get in hand-ready consolidated information on Pharmaceutical Quality guidelines, Quality metrics, and implementation of simplified SOP guidelines, plant layouts to implement Quality metrics for Pharmaceutical Manufacturing systems in tablets, capsules, liquid orals, and semi-solid dosage forms.
The chapters cover the various aspects of Pharmaceutical Quality Assurance. The selection of topics is mainly based on the requirements of Pharmaceutical regulatory guidelines of India, the UK, the USA, Australia, and South Africa. Each chapter includes the abstract, detailed explanation, implementation guidelines, flowcharts, layouts, and Standard Operating Procedure of quality metrics for the Pharmaceutical Manufacturing System
Autoren-Porträt
Dr. Minal R. Ghante is presently working as I/c Principal and professor in Smt. Kashibai Navale College of Pharmacy, Pune. Her research areas include Quality Assurance, regulatory audits, drafting of Validation Protocols, Analytical method development, and validation by HPLC, LC-MS/MS, HPTLC, and Stability/Degradation Studies of APIs & Pharmaceutical Products. She has over 18 years of teaching and research experience at the undergraduate & postgraduate levels. She has more than 35 research publications in various Journals of National & International repute & authored/co-authored 12 books to her credit. She has presented more than 30 posters in multiple symposia/conferences. She is a recognized Ph.D. guide & Postgraduate Teacher at Savitribai Phule Pune University; 40 PG students have completed dissertations under her guidance.
Dr. Manohar Anant Potdar is currently a Professor Emeritus in Smt. Kashibai Navale College ofPharmacy, Pune. His research areas include Plant Design and Operation, Production planning and Control systems, Pharmaceutical Validation, Good Manufacturing Practices, Plant Administration, Quality Assurance Techniques, Quality Planning and Analysis., Quality Management Systems, Pharmaceutical Quality Audits, and Regulatory Affairs. He has 33 years of industrial experience and ten years of teaching experience. He has authored nine technical books and nine library books. He is an approved guide for M.Pharm and Ph.D. and has mentored 34 M. Pharm students and one Ph.D. student for dissertation work. He is an expert in Production and Operation Management, Quality Assurance and Validation-Audits, Project Management, and Employee Training.
Dr. Vidhya Bhusari is an Associate Professor in Smt. Kashibai Navale College of Pharmacy, Pune. She has completed her Ph. D & M. Pharm from Bharati Vidyapeeth University, Pune, and has secured M. Pharm first classwith distinction. Her research areas
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include Quality Assurance, Analytical Method Development, and Validation by HPLC, LC-MS/MS, HPTLC, and Stability/Degradation Studies of APIs & Pharmaceutical Products. She has around five years of teaching experience and about six years of industrial experience. She has more than 40 research publications in various journals of International repute. She has authored one book to her credit. She has presented five posters and papers in multiple symposia/conferences. She has guided 12 M. Pharm students for their dissertation.
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Bibliographische Angaben
- 2024, 2024, 523 Seiten, Englisch
- Herausgegeben: Minal Ghante, Manohar Potdar, Vidhya Bhusari
- Verlag: Springer Nature Singapore
- ISBN-10: 9819992710
- ISBN-13: 9789819992713
- Erscheinungsdatum: 11.03.2024
Abhängig von Bildschirmgröße und eingestellter Schriftgröße kann die Seitenzahl auf Ihrem Lesegerät variieren.
eBook Informationen
- Dateiformat: PDF
- Größe: 13 MB
- Ohne Kopierschutz
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Sprache:
Englisch
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