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How to Integrate Quality by Efficient Design (QbED) in Product Development - (Expertise in Pharmaceutical Process Technology) by Bhavishya Mittal

How to Integrate Quality by Efficient Design (QbED) in Product Development - (Expertise in Pharmaceutical Process Technology) by  Bhavishya Mittal - 1 of 1
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Highlights

  • The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns.
  • Author(s): Bhavishya Mittal
  • 274 Pages
  • Business + Money Management, Industries
  • Series Name: Expertise in Pharmaceutical Process Technology

Description



About the Book



"The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns. Unfortunately, despite large resources spent on R&D, multifactor productivity of pharmaceuticals is on the decline for several years now. Because of this business reality, pharmaceutical companies have seen a notable change in the traditional operating model and footprint over the past couple of decades. Outsourcing, in particular, has emerged as a successful business model for many pharmaceutical companies looking for ways to strategically increase their R&D capabilities and to augment their in-house resources. How to Integrate Quality by Efficient Design (QbED) in Product Development bridges the gap between theory and practice when it comes to strategic decision-making in a pharmaceutical research scenario. This book will introduce the concept of QbED and focus on various aspects such as patient-centric product designs, platform-based manufacturing technologies, business acuity, and regulatory strategies to balance the challenges in outsourcing with the need for strategic and statistically sound experiments rooted in good science. Detailed discussions will cover pharmaceutical business models, regulatory approval process, quality by design (QbD), business analytics, and manufacturing excellence specifically for small molecules and solid oral dosage forms. With the addition of case studies, flowcharts, diagrams, and data visualizations, How to Integrate Quality by Efficient Design (QbED) in Product Development will be a practical reference to help professionals working in the area of pharmaceutical drug development, strategy, and outsourcing management"--



Book Synopsis



The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing business-related concerns. Unfortunately, despite large resources spent on R&D, multifactor productivity of pharmaceuticals is on the decline for several years now. Because of this business reality, pharmaceutical companies have seen a notable change in the traditional operating model and footprint over the past couple of decades. Outsourcing, in particular, has emerged as a successful business model for many pharmaceutical companies looking for ways to strategically increase their R&D capabilities and to augment their in-house resources. How to Integrate Quality by Efficient Design (QbED) in Product Development bridges the gap between theory and practice when it comes to strategic decision-making in a pharmaceutical research scenario. This book will introduce the concept of QbED and focus on various aspects such as patient-centric product designs, platform-based manufacturing technologies, business acuity, and regulatory strategies to balance the challenges in outsourcing with the need for strategic and statistically sound experiments rooted in good science. Detailed discussions will cover pharmaceutical business models, regulatory approval process, quality by design (QbD), business analytics, and manufacturing excellence specifically for small molecules and solid oral dosage forms. With the addition of case studies, flowcharts, diagrams, and data visualizations, How to Integrate Quality by Efficient Design (QbED) in Product Development will be a practical reference to help professionals working in the area of pharmaceutical drug development, strategy, and outsourcing management.

  • Part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin
  • Integrates pharmaceutical business models, economics, and outsourcing-related challenges into pharmaceutical product development
  • Discusses relevant literature references in quality risk management, business strategy, QbD, and product development
  • Provides decision-making flowcharts, conceptual diagrams, and data visualizations to make the book useful, easy to read, and to understand
Dimensions (Overall): 9.0 Inches (H) x 6.0 Inches (W) x .58 Inches (D)
Weight: .82 Pounds
Suggested Age: 22 Years and Up
Series Title: Expertise in Pharmaceutical Process Technology
Sub-Genre: Industries
Genre: Business + Money Management
Number of Pages: 274
Publisher: Academic Press
Theme: Pharmaceutical & Biotechnology
Format: Paperback
Author: Bhavishya Mittal
Language: English
Street Date: September 2, 2019
TCIN: 94138860
UPC: 9780128168134
Item Number (DPCI): 247-30-6635
Origin: Made in the USA or Imported
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Shipping details

Estimated ship dimensions: 0.58 inches length x 6 inches width x 9 inches height
Estimated ship weight: 0.82 pounds
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