Chapter 5. Good Manufacturing Practices
Published Online: 24 DEC 2009
DOI: 10.1002/9780470773031.ch5
Copyright © 2008 John Wiley & Sons, Ltd
Book Title
Quality Systems and Controls for Pharmaceuticals
Additional Information
How to Cite
Sarker, D. K. (2009) Good Manufacturing Practices, in Quality Systems and Controls for Pharmaceuticals, John Wiley & Sons, Ltd, Chichester, UK. doi: 10.1002/9780470773031.ch5
Publication History
- Published Online: 24 DEC 2009
- Published Print: 15 AUG 2008
ISBN Information
Print ISBN: 9780470056929
Online ISBN: 9780470773031
- Summary
- Chapter
Keywords:
- good manufacturing practice (cGMP);
- pharmaceutical products and GMP considerations;
- standard product manufacture;
- droplet size maintenance and product stability;
- emulsion and dispersion stability;
- material manufacture and specialised production facilities;
- colloidal mixtures and biomedical nanotechnology;
- chemotherapeutic nanoparticles and clinical trials;
- nuclear clinical medicine and radiopharmaceutical use - therapy and diagnostics
Summary
This chapter contains sections titled:
Manufacture of standard products
Manufacture of materials requiring specialised production facilities
Quality assurance aspects of medical gases, devices and miscellaneous product manufacture