Good Design Practices for GMP Pharmaceutical Facilities
eBook - ePub

Good Design Practices for GMP Pharmaceutical Facilities

  1. 518 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Good Design Practices for GMP Pharmaceutical Facilities

Book details
Table of contents
Citations

About This Book

This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical manufacturing which include strategies for sustainability and LEED building ratings. All chapters have been re-examined with a fresh outlook on current good design practices.

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Yes, you can access Good Design Practices for GMP Pharmaceutical Facilities by Terry Jacobs, Andrew A. Signore in PDF and/or ePUB format, as well as other popular books in Medicine & Pharmacology. We have over one million books available in our catalogue for you to explore.

Information

Publisher
CRC Press
Year
2016
ISBN
9781315355023
Edition
2
Topic
Medicine
Subtopic
Pharmacology

Table of contents

  1. Cover
  2. Half Title
  3. Title Page
  4. Copyright Page
  5. Dedication
  6. Table of Contents
  7. Preface
  8. Acknowledgments
  9. Editors
  10. Contributors
  11. Introduction
  12. Chapter 1 Pharmaceutical Industry Profile
  13. Chapter 2 Current Good Manufacturing Practices
  14. Chapter 3 Legacy Facility Master Planning
  15. Chapter 4 Architectural Design Issues
  16. Chapter 5 Facility Utility Systems
  17. Chapter 6 High-Purity Water
  18. Chapter 7 Commissioning, Qualification, and Validation
  19. Chapter 8 Process Engineering
  20. Chapter 9 Oral Solid Dosage Facilities
  21. Chapter 10 Continuous Oral Solid Dose Processing
  22. Chapter 11 Sterile Manufacturing Facilities
  23. Chapter 12 Biotechnology Facilities
  24. Chapter 13 Codes and Standards
  25. Chapter 14 Containment Technology
  26. Chapter 15 Occupational Health and Safety
  27. Chapter 16 Sustainability
  28. Chapter 17 QA/QC Laboratories and Related Support Spaces
  29. Chapter 18 Packaging and Warehousing
  30. Appendix I: Novel Drug Delivery
  31. Appendix II: Biopharmaceutical Factories of the Future
  32. Index