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

Autor Bhavishya Mittal
en Limba Engleză Paperback – 27 aug 2019
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
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Specificații

ISBN-13: 9780128168134
ISBN-10: 0128168137
Pagini: 274
Ilustrații: Illustrated
Dimensiuni: 151 x 229 mm
Greutate: 0.37 kg
Editura: ELSEVIER SCIENCE
Seria Expertise in Pharmaceutical Process Technology


Public țintă

Pharmaceutical professionals and scientists working the area of pharmaceutical drug development, manufacturing, regulations, strategy, and outsourcing management

Cuprins

1. Health Care: A Societal Benchmark2. Pharmaceuticals: A Highly Innovative Business3. Pharmaceutical Productivity: Challenges and Opportunities4. QbD: A Welcome Evolution5. QbED: An Emerging Concept6. Adaptive Product Designs: A Wave of the Future7. Patient-Centric Drug Product Designs: A Business Necessity8. Manufacturing Excellence: Only Road to Continual Improvement9. Case Studies and Supplemental Resources