Generic Drug Development: Principles, Practices, and Global Trends
| AUTHOR | Hemendra Gautam, Sunita Dahiya; Dr Rajiv Dahiya; Dr Saurabh Dahiya |
| PUBLISHER | Notion Press (03/25/2025) |
| PRODUCT TYPE | Hardcover (Hardcover) |
Generic Drug Development: Principles, Practices, and Global Trends" is a comprehensive and cutting-edge guide to understanding the complex world of generic drug development. Edited by Dr. Sunita Dahiya, Associate Professor at the University of Puerto Rico, San Juan, PR, USA, this book brings together a wealth of knowledge and expertise in the field, offering an in-depth exploration of the principles, practices, and emerging trends that shape the development and approval of generic medicines.
With contributions from a team of experts:
Dr. Saurabh Dahiya, Associate Professor at Delhi Pharmaceutical Sciences and Research University, India, delves into the latest innovations in drug design and formulation techniques for generics.
Dr. Rajiv Dahiya, Professor at The University of the West Indies, St. Augustine, Trinidad & Tobago, brings a global perspective on pharmaceutical regulations and generic drug market trends.
Dr. Hemendra Gautam, Professor from Bareilly, Uttar Pradesh, India, provides a deep dive into regulatory frameworks and bioequivalence studies in the generic drug development process.
This book is an essential resource for students, researchers, and professionals in the pharmaceutical field, focusing on the challenges, innovations, and regulatory complexities involved in generic drug development.
Generic Drug Development: Principles, Practices, and Global Trends" is a comprehensive and cutting-edge guide to understanding the complex world of generic drug development. Edited by Dr. Sunita Dahiya, Associate Professor at the University of Puerto Rico, San Juan, PR, USA, this book brings together a wealth of knowledge and expertise in the field, offering an in-depth exploration of the principles, practices, and emerging trends that shape the development and approval of generic medicines.
With contributions from a team of experts:
Dr. Saurabh Dahiya, Associate Professor at Delhi Pharmaceutical Sciences and Research University, India, delves into the latest innovations in drug design and formulation techniques for generics.
Dr. Rajiv Dahiya, Professor at The University of the West Indies, St. Augustine, Trinidad & Tobago, brings a global perspective on pharmaceutical regulations and generic drug market trends.
Dr. Hemendra Gautam, Professor from Bareilly, Uttar Pradesh, India, provides a deep dive into regulatory frameworks and bioequivalence studies in the generic drug development process.
This book is an essential resource for students, researchers, and professionals in the pharmaceutical field, focusing on the challenges, innovations, and regulatory complexities involved in generic drug development.