Handbook of Biological Therapeutic Proteins
eBook - ePub

Handbook of Biological Therapeutic Proteins

Regulatory, Manufacturing, Testing, and Patent Issues

  1. 412 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Handbook of Biological Therapeutic Proteins

Regulatory, Manufacturing, Testing, and Patent Issues

About this book

Since 1972, which marks the invention of recombinant engineering, more than 500 therapeutic proteins have been approved for clinical use. Today, biological drugs constitute almost 70% of all new drugs and have a biological origin. The first edition of this book dealt with biosimilars, and this edition (i.e., the second edition) focuses on new drugs, yet limits to therapeutic proteins. Newer technologies for drug development represent the updated topics in the book and include repur-posing, AI- driven identification of newer designs, novel expression systems, manufacturing using these systems, rapidly changing regulatory pathways, and legal hurdles. This edition discusses how to identify, develop, manufacture, and take multibillion dollar products to market within the shortest possible time.

Features:

  • Complete and thorough coverage of the regulatory and technological challenges of developing generic therapeutic proteins
  • Comprehensive, discovery to market, newer technologies, regulatory planning and IP hurdles are included that are not found elsewhere
  • Expanded volume that must be in the hands of every company interested in biological drugs, including the mRNA-based biopharmaceutical companies fast appearing on the market
  • Discusses how to identify, develop, manufacture, and take multibillion dollar products to market in the shortest possible time
  • Renowned author and entrepreneur in the field of drug discovery and production

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Yes, you can access Handbook of Biological Therapeutic Proteins by Sarfaraz Niazi in PDF and/or ePUB format, as well as other popular books in Medicine & Biochemistry in Medicine. We have over one million books available in our catalogue for you to explore.

Information

Table of contents

  1. Cover
  2. Half-Title Page
  3. Title Page
  4. Copyright Page
  5. Table of Contents
  6. Preface
  7. 1 Overview of the Development of Biosimilar Biopharmaceuticals
  8. 2 Regulatory Requirements for a Proposed Biosimilar Product
  9. 3 Development of a Master Plan for the Biosimilar
  10. 4 Trends in the Manufacturing of Recombinant Proteins
  11. 5 Analytical Assessment of a Biosimilar
  12. 6 Clinical Pharmacology Assessment of a Proposed Biosimilar
  13. 7 Clinical Immunogenicity Assessment of the Biosimilar
  14. 8 Clinical Efficacy Assessment of the Proposed Biosimilar
  15. 9 Recombinant Manufacturing System for Biopharmaceuticals
  16. 10 Upstream Processes Involved in Protein Production
  17. 11 Downstream Processes Involved in Protein Production
  18. 12 Formulation of Biopharmaceuticals
  19. 13 Quality and Compliance Systems
  20. 14 Intellectual Property Issues for Scientists
  21. Bibliography
  22. Index